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Live online
Classroom
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2025 |
2026 |
| Nov |
Dec |
Jan |
Feb |
Mar |
Apr |
May |
Jun |
Jul |
Aug |
Sep |
Oct |
| A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products |
Animal Health |
4 |
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7 |
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| A Practical Approach to Veterinary Vaccine Development and Registration in the EU |
Animal Health |
6-7 |
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10-11 |
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23-24 |
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| A Practical Guide to Producing and Maintaining the PSMF |
Pharmaceutical |
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13 |
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16 |
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| A Practical Guide to Writing Risk Management Plans (RMPs) |
Pharmaceutical |
12 |
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20 |
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19 |
| A Practical Introduction to Good Clinical Practice (GCP) |
Pharmaceutical |
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15 |
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6 |
| A Practical Overview of Pre-Filled Syringes |
Medical Devices |
5-6 |
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11-12 |
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| A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK |
Medical Devices |
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29 |
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20 |
| AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects |
Artificial Intelligence (AI) in Life Sciences |
6 |
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6 |
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| AI in Pharmacovigilance |
Artificial Intelligence (AI) in Life Sciences |
19 |
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| Achieving Publication Success in Scientific Journals |
Pharmaceutical |
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2 |
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21 |
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| Additional Risk Minimization Measures (aRMMs) and Their Effectiveness |
Pharmaceutical |
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3 |
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| Advanced Pharmacovigilance: From Performing Successful Due Diligence to Benefit-Risk Assessments – What to Consider |
Pharmaceutical |
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23-25 |
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21-25 |
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| Advanced Veterinary Pharmacovigilance |
Animal Health |
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21-22 |
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| An Essential Overview of Medical Information |
Pharmaceutical |
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4 |
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22 |
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| An Essential Overview of the Pharmaceutical and Biotech Industries |
Pharmaceutical |
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12 |
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28 |
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| An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices |
Medical Devices |
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14 |
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| An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals |
Pharmaceutical |
20 |
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8 |
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| An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices |
Medical Devices |
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21 |
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| An Introduction to Signal Detection |
Pharmaceutical |
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16 |
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14 |
| An Introduction to Technology Transfer for Solid Dosage Forms |
Pharmaceutical |
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6 |
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18 |
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| An Introduction to the Design and Development of Medical Devices |
Medical Devices |
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3-4 |
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29-30 |
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| An Overview of EU and UK Regulatory Affairs |
Pharmaceutical |
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11-12 |
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21-22 |
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| An Overview of Ethical Standards in Clinical Research Publication |
Pharmaceutical |
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13 |
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| An introduction to Risk Management ISO 14971:2019 |
Medical Devices |
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27 |
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20 |
| Animal Feed and Feed Additive Registration in China and Thailand |
Animal Health |
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16 |
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22 |
| Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions |
Pharmaceutical |
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10 |
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10 |
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| Best Practice for Writing Effective SOPs |
Pharmaceutical |
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4 |
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26 |
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14 |
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| Best Practices for Supplier Qualification in Life Science |
Pharmaceutical |
13-14 |
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6-7 |
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| Biological Evaluation of Medical Devices |
Medical Devices |
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21-22 |
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13-14 |
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| Biosimilars |
Pharmaceutical |
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16-17 |
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22-23 |
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| Biotechnology for the Non-Biotechnologist |
Pharmaceutical |
10-14 |
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| Building The Business Case For Pharma 4.0 |
Pharmaceutical |
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13 |
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6 |
| CAPA (Corrective and Preventative Action) |
Pharmaceutical |
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5 |
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15 |
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| Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products |
Pharmaceutical |
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23-24 |
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19-20 |
| Cleaning Validation - Best Practice in Pharmaceuticals |
Pharmaceutical |
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2-3 |
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23-24 |
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| Cleanroom Requirements for Medical Device Manufacturers |
Medical Devices |
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23 |
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21 |
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| Clinical & Post-Marketing Safety |
Pharmaceutical |
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11-12 |
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| Clinical Evaluation of Medical Device Software and Software as a Medical Device |
Medical Devices |
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28 |
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1 |
| Clinical Evaluation of Medical Devices: The Clinical Evaluation Report |
Medical Devices |
25-26 |
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| Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application |
Pharmaceutical |
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16-17 |
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30-1 |
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| Clinical Quality Management Systems |
Pharmaceutical |
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23-24 |
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17-18 |
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| Clinical Research Project Management |
Pharmaceutical |
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29-1 |
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21-23 |
| Clinical Trial Agreements: Key Legal, Regulatory and IP Considerations for the EU and UK Markets |
Pharmaceutical |
28 |
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18 |
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2 |
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| Clinical Trial Monitoring |
Pharmaceutical |
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29-30 |
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| Clinical Trial Regulatory Requirements |
Pharmaceutical |
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2-3 |
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14-15 |
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| Competition Law for the Pharmaceutical Industry |
Pharmaceutical |
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27 |
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| Conflict Management for Pharmaceutical Executives |
Leadership & Management for Life Sciences |
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26-29 |
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13-16 |
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| Cosmetovigilance |
Cosmetics |
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18-19 |
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| Cyber Security for Medical Devices |
Medical Devices |
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19-20 |
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28-29 |
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| Data Integrity Auditor Masterclass |
Pharmaceutical |
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22-23 |
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14-15 |
| Data Integrity and Document Management |
Pharmaceutical |
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11 |
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22 |
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| Dealing With Scientific Journal Reviewers: From Comments to Resubmission |
Pharmaceutical |
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15 |
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| Development of Combination Products: Critical Interactions |
Pharmaceutical |
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9-10 |
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16-17 |
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| Digital CMC |
Pharmaceutical |
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6 |
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| Digital CMC: The Key To Realising Pharma 4.0 |
Pharmaceutical |
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1 |
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23 |
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| Digital Technology Transfers |
Pharmaceutical |
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4 |
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22 |
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| Digital Technology and Personalisation in Patient Support Programmes |
Pharmaceutical |
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6 |
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| Drafting Commercial Contracts for the Pharmaceutical Industry |
Pharmaceutical |
12-13 |
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20-21 |
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| EU Pharmaceutical Regulations and Strategy |
Pharmaceutical |
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2-3 |
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5-6 |
| EU Proposed Pharmaceutical Legislation Changes |
Pharmaceutical |
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19 |
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1 |
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| Effective Change Management in Pharma |
Pharmaceutical |
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17 |
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9 |
| Effective Communication & Negotiation in Technology Transfers |
Pharmaceutical |
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18 |
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15 |
| Effective Deviation Management Systems in Pharma |
Pharmaceutical |
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20 |
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25 |
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| Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains |
Pharmaceutical |
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15 |
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| Effective Technical Writing & Editing |
Pharmaceutical |
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15 |
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| Ensuring Clinical Research Quality & Patient Safety |
Pharmaceutical |
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2 |
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14 |
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| Essential Documentation Skills for Clinical Research Compliance |
Pharmaceutical |
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9 |
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5 |
| FDA Approval Process for Medical Devices |
Medical Devices |
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2-3 |
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30-1 |
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| GCP and Clinical Research Update - Hot Inspection Topics |
Pharmaceutical |
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19 |
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| GMP Principles in Vaccine Manufacturing |
Pharmaceutical |
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10-11 |
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16-17 |
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| Global Market Access for Medical Device Software |
Medical Devices |
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8-9 |
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| Golden Rules of Being a Successful GMP Auditor |
Pharmaceutical |
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5-6 |
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30-1 |
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| Good Distribution Practices of Pharmaceuticals and APIs |
Pharmaceutical |
17-18 |
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14-15 |
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| Good Writing Practice for Clinical Research: Ethics, Standards & Compliance |
Pharmaceutical |
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20 |
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| How to Audit Pharmaceutical Suppliers (Material and Service) |
Pharmaceutical |
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26-27 |
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14-15 |
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| How to Deal with Difficult Situations in GMP Audits |
Pharmaceutical |
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5 |
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28 |
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| How to Interview During GMP Audits |
Pharmaceutical |
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12 |
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24 |
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| How to Manage Internal GMP Audits |
Pharmaceutical |
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24-25 |
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21-22 |
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| How to Pass International Health Authority Inspections |
Pharmaceutical |
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16-17 |
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7-8 |
| How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits |
Pharmaceutical |
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3-4 |
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18-19 |
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| Interpersonal Project Management Skills for the Life Sciences Industries |
Leadership & Management for Life Sciences |
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22-23 |
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16-17 |
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| Introduction to Veterinary Pharmacovigilance |
Animal Health |
5-6 |
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9-10 |
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16-17 |
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| Introduction to the In-Vitro Diagnostic Regulation (IVDR) |
Medical Devices |
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16-17 |
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15-16 |
| Literature Searching in Drug Safety |
Pharmaceutical |
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14-15 |
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| MBA Strategic Thinking for Pharma and Biopharma Professionals |
Leadership & Management for Life Sciences |
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23-24 |
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21-22 |
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| Managing Human Error: A Strategic Approach for Pharmaceutical Managers |
Leadership & Management for Life Sciences |
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28 |
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1 |
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| Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 |
Pharmaceutical |
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13-14 |
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15-16 |
| Masterclass: Market Authorisation of AI-enabled Medical Devices |
Artificial Intelligence (AI) in Life Sciences |
18-19 |
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29-30 |
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| Mastering CTD Submissions in the MENA Region |
Pharmaceutical |
28 |
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19 |
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| Mastering Ethical and Effective Scientific Publishing: Applying Good Publication Practice (GPP) |
Pharmaceutical |
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20 |
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8 |
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| Mastering Grant Writing: Essential Skills for Crafting Winning Proposals |
Pharmaceutical |
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22-23 |
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| Measuring Performance in Clinical Research Management |
Pharmaceutical |
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6 |
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| Medical Device Regulation in the Eurasian Union, Russia and the CIS |
Medical Devices |
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9-10 |
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30-1 |
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| Medical Device Regulations in Asia-Pacific Markets |
Medical Devices |
3-4 |
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3-4 |
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16-17 |
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| Medical Device Regulations in the Middle East and North Africa |
Medical Devices |
19-20 |
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18-19 |
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| Medical Device Single Audit Programme (MDSAP) |
Medical Devices |
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25-26 |
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| Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations |
Medical Devices |
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26-30 |
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22-26 |
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| Medical Editing for Peer-Reviewed Journals |
Pharmaceutical |
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8 |
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| Medical Writing Excellence: Crafting Compelling Scientific Documents |
Pharmaceutical |
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4-5 |
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30-1 |
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| Medical Writing for Consumers |
Pharmaceutical |
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21 |
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1 |
| Medical Writing for Medical Devices |
Medical Devices |
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25-26 |
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| Medical Writing with AI |
Artificial Intelligence (AI) in Life Sciences |
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18 |
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| Metered Dose Inhaler (MDI) Technology |
Medical Devices |
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27-28 |
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7-8 |
| Microbiomics in Clinical Trials |
Pharmaceutical |
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26 |
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14 |
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| Modern Agile Leadership for Pharma and Biopharma Professionals: Adapting to a Changing Workplace |
Leadership & Management for Life Sciences |
17-18 |
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11-12 |
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| Molecular Biology for the Non-Molecular Biologist |
Pharmaceutical |
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20-21 |
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8-9 |
| Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products |
Pharmaceutical |
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2-3 |
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14-15 |
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| Navigating ICH GCP E6 (R3): What You Need to Know |
Pharmaceutical |
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29 |
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13 |
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| Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests |
Medical Devices |
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15 |
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| New EU GMP Annex 1: Compliant Aseptic Operations |
Pharmaceutical |
25-27 |
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19-21 |
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| Non-Conformance and Corrective Action for Medical Device Manufacturers |
Medical Devices |
|
11 |
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19 |
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| Orphan Drug Regulatory Masterclass: EU & US Insights |
Pharmaceutical |
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4 |
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6 |
| Pharmaceutical Development of ATMPs |
Pharmaceutical |
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18-19 |
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28-29 |
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| Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success |
Pharmaceutical |
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26-28 |
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6-8 |
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| Pharmaceutical Regulatory Affairs in Africa |
Pharmaceutical |
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6-7 |
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| Pharmaceutical Regulatory Affairs in Asia |
Pharmaceutical |
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24-26 |
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20-22 |
| Pharmaceutical Regulatory Affairs in China |
Pharmaceutical |
26-27 |
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3-4 |
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| Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union |
Pharmaceutical |
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5-6 |
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30-1 |
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| Pharmaceutical Regulatory Affairs in the Middle East |
Pharmaceutical |
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24-25 |
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20-21 |
| Pharmacovigilance Aspects of Licensing Agreements |
Pharmaceutical |
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1-2 |
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25 |
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| Pharmacovigilance QMS & Inspection Preparation |
Pharmaceutical |
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27-28 |
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8-9 |
| Pharmacovigilance: An Overview of Drug Safety from Safety Collection to Regulatory Inspection |
Pharmaceutical |
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30 |
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5-6 |
| Positive Persuading and Influencing Skills for Pharma Professionals |
Leadership & Management for Life Sciences |
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18-21 |
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| Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) |
Medical Devices |
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10-11 |
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| Practical Implementation of GCP in Veterinary Field Studies |
Animal Health |
25-26 |
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13-14 |
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| Practical Requirements of the Arab Pharmacovigilance Guidelines |
Pharmaceutical |
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21-22 |
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21-22 |
| Process Validation for Medical Devices |
Medical Devices |
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4-5 |
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| Project Management for Pharma Professionals |
Leadership & Management for Life Sciences |
10-11 |
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9-10 |
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2-3 |
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| Protein Engineering for Pharmaceutical Biotechnology |
Pharmaceutical |
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21-22 |
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7-8 |
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| Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in Pharma |
Artificial Intelligence (AI) in Life Sciences |
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22 |
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| Registration of Veterinary Pharmaceuticals in China |
Animal Health |
|
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16 |
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22 |
| Regulatory Compliance and Safety Standards for Aesthetic Devices |
Cosmetics |
|
5 |
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12 |
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| Root Cause Analysis and Critical Thinking |
Leadership & Management for Life Sciences |
24 |
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18 |
|
|
|
|
|
| Selecting the Best Scientific Journal for Your Research |
Pharmaceutical |
|
|
|
|
|
13 |
|
|
|
|
|
19 |
| Signal Detection and Regulatory Expectations |
Pharmaceutical |
|
|
|
2-3 |
|
|
|
|
|
|
30-1 |
|
| Signal Detection: A Comprehensive Introduction |
Pharmaceutical |
|
|
28 |
|
|
|
|
|
1 |
|
|
|
| Smart Packaging and Electronic Patient Information |
Pharmaceutical |
|
|
|
|
|
|
15 |
|
|
|
|
|
| Software Automation in Research and Development (R&D) Clinical Trials |
Pharmaceutical |
|
|
|
|
17 |
|
|
|
|
|
28 |
|
| Stability Testing of Pharmaceuticals and Biopharmaceuticals |
Pharmaceutical |
10-11 |
|
|
|
|
|
20-21 |
|
|
|
|
|
| Sterilization of Medical Devices |
Medical Devices |
|
|
|
|
|
23-24 |
|
|
|
|
|
15-16 |
| Successful Cognitive Testing in Clinical Drug Trials: Biomarkers, Test Selection & Integration |
Pharmaceutical |
|
|
|
|
16 |
|
|
|
|
|
18 |
|
| Successful Medical Writing – from Protocol to CTD |
Pharmaceutical |
|
|
|
|
23-24 |
|
|
|
|
|
22-23 |
|
| Sustainable Product Design for MedTech Engineers and Developers |
Medical Devices |
|
|
|
|
|
|
7-8 |
|
|
|
|
|
| The 2024 EU AI Act |
Artificial Intelligence (AI) in Life Sciences |
|
|
|
|
|
|
|
23 |
|
|
|
|
| The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA |
Animal Health |
|
|
|
|
|
|
|
15-18 |
|
|
|
|
| The Applications of Nanoparticles in the Pharmaceutical and Biomedical Industries |
Pharmaceutical |
|
|
|
|
11-12 |
|
|
|
|
|
15-16 |
|
| The Common Technical Document |
Pharmaceutical |
24-25 |
|
27-28 |
|
|
|
14-15 |
|
|
|
|
21-22 |
| The FDA Drug Approval Process |
Pharmaceutical |
|
|
|
23-24 |
|
|
|
|
|
|
24-25 |
|
| The Future of Manufacturing: 3D Printing for Medical Devices |
Medical Devices |
|
10 |
|
|
|
|
|
17 |
|
|
|
|
| The Pharma Mini MBA |
Leadership & Management for Life Sciences |
5-7 |
|
|
|
18-20 |
|
|
|
8-10 |
|
|
|
| The Principles & Applications of CRISPR |
Pharmaceutical |
|
|
23 |
|
|
|
|
|
7 |
|
|
|
| The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry |
Pharmaceutical |
|
|
|
|
|
20-21 |
|
|
|
|
|
12-13 |
| The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR |
Medical Devices |
|
|
|
|
4 |
|
|
|
|
|
21 |
|
| Thinking Outside of the GMP Box |
Pharmaceutical |
|
|
|
3-4 |
|
|
|
|
|
|
16-17 |
|
| UK Conformity Assessed (UKCA) Marking for Medical Devices |
Medical Devices |
|
|
|
|
|
15 |
|
|
|
|
|
21 |
| US FDA - Understanding Key Factors When Working with the FDA |
Pharmaceutical |
26 |
|
|
|
|
|
12 |
|
|
|
|
|
| Understanding Active Pharmaceutical Ingredients (APIs) |
Pharmaceutical |
|
|
|
|
|
29-30 |
|
|
|
|
|
21-22 |
| Understanding Computer System Validation (CSV) |
Pharmaceutical |
24-25 |
|
|
|
|
|
|
17-18 |
|
|
|
|
| Understanding Scientific Journal Submission and Publication |
Pharmaceutical |
|
|
|
|
|
|
11 |
|
|
|
|
|
| Understanding Toxicology: A Guide for Non-Toxicologists |
Pharmaceutical |
|
|
19 |
|
|
|
|
|
15 |
|
|
|
| Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers |
Medical Devices |
|
|
|
|
|
|
|
8 |
|
|
|
|
| Upstream and Downstream Manufacturing in the Biopharmaceutical Industry |
Pharmaceutical |
|
5 |
|
|
|
|
|
11 |
|
|
|
|
| Utilising Patient Adherence Data and Digital Tools to Improve Patient Outcomes |
Pharmaceutical |
|
|
|
|
|
16 |
|
|
|
|
|
13 |
| Variations to Marketing Authorisations |
Pharmaceutical |
|
|
|
|
|
|
|
2-3 |
|
|
|
|
| Veterinary Pharmaceutical Submissions in the EU |
Animal Health |
25-26 |
|
|
|
|
|
18-19 |
|
|
|
|
|
| Working with Emotional Intelligence in the Pharmaceutical and Biopharma Industry |
Leadership & Management for Life Sciences |
|
|
|
|
|
27 |
|
|
|
|
|
19 |