Search results: pharmaceutical

Covering Bahrain, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Oman, Palestine, Qatar, Saudi Arabia, Sudan, Syria, UAE and Yemen

A detailed overview of the key areas of pharmaceutical regulatory affairs in China, Hong Kong, Macau and Taiwan.

Covering the key regions of South Africa, Namibia, Zimbabwe, Zambia, Malawi, Tanzania, Kenya, Uganda, Nigeria, Ghana and Maghreb countries - Algeria, Morocco, Tunisia

This seminar will provide an overview of the key areas of pharmaceutical regulatory affairs in Asia including, China, Hong Kong SAR, Brunei, the Philippines, India, Indonesia, Malaysia, Singapore, Thailand, Cambodia, Laos, Vietnam, Taiwan, Korea, Japan

This interactive course will discuss the regulatory requirements for human pharmaceuticals within these regions, and discuss the implications of the new joint Eurasian Union regulation.

Master pharmaceutical packaging essentials in 3 days: materials selection, regulatory compliance, and testing requirements. Led by industry expert with 25+ years' experience.

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.

Covering Bahrain, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Oman, Palestine, Qatar, Saudi Arabia, Sudan, Syria, UAE, Yemen, Tunisia, Morocco and Algeria.

The course will provide an up-to-date overview of the current European pharmaceutical regulatory environment including procedures for obtaining marketing authorisation and post-approval obligations. Political agreement on the proposed changes to the EU pharmaceutical legislation has been reached and projected implementation and transition timelines will be discussed in the relevant sections and impact on strategic considerations for obtaining and maintaining marketing authorisations. Procedures for obtaining marketing authorisations in the UK will be discussed.

This course will provide an up-to-date overview of current European pharmaceutical legislation and the regulatory impact of the proposed changes.

This training provides knowledge and practical skills to effectively audit material and service providers, covering key areas including raw materials, contract manufacturing, logistics, and packaging.

Drafting successful pharmaceutical patents is complex and there are many pitfalls and risks to be aware of. You need to ensure you’re maximising the protection for your, and your client’s, pharmaceutical inventions thorough both primary and secondary pharmaceutical patents.

Design efficient stability studies that are suitable for global marketing. Be able to carry out appropriate stability studies and manage stability samples and facilities, learn how to save resources on stability testing and improve the likelihood of regulatory approval of stability protocols.

Advance your expertise in protein engineering with this comprehensive course. Learn cutting-edge techniques in therapeutic development, biotechnology applications, and regulatory compliance, ideal for professionals in pharmaceutical and industrial sectors.

This highly effective four module webinar aims to help delegates to develop and hone their skills in resolving and managing conflict.

A one-day practical and interactive seminar focuses on everything you need to know about competition law and the pharmaceutical sector

Learn how to navigate the regulatory system of veterinary pharmaceuticals in China.

This programme will give you an invaluable overview of the pharmaceutical industry, from discovery of the molecule through development to marketing.

Gain a comprehensive understanding of industry-leading practices, ensuring precision in distribution from manufacturer to end user. Navigate complex supply chains, focus on compliance, and elevate your commitment to quality assurance throughout the entire distribution process.

This course will cover the key regulations used globally in human factors and usability engineering: the specific standards and guidances, methods, and the tools commonly used in medical device development.

Master the principles of cleaning validation to ensure pharmaceutical manufacturing equipment meets stringent regulatory standards, preventing contamination and safeguarding public health.

Attendees will gain a comprehensive understanding of the science behind nanoparticles, their diverse applications, manufacturing and the opportunities and challenges involved in bringing nanoparticle-based solutions to market.

Gain essential financial fluency for today’s complex pharma environment. This intensive two-day course helps non-financial leaders interpret P&L, manage compliance, and link strategic, operational, and regulatory decisions to financial performance

This course will help participants learn to communicate and influence more effectively within the pharma and biopharma industries.

An indepth look at how leaders can enhance their effectiveness in health and safety by reducing risk, preventing incidents, and mastering communication and human-error management to avoid costly failures and build a resilient safety culture.

Transform your approach to managing human error with evidence-based insights. Essential training for managers covering cognitive biases, process improvement and organisational communication failures.

In this talk, explore the fundamental concepts, techniques, and processes that make up the backbone of biomanufacturing, pharmaceutical production, and biotechnology.

In this webinar, we will discuss the major requirements and strategies for nitrosamines, a hot topic that is on the forefront of many company's minds.

A two-day seminar providing an essential overview of biosmilars and how they differ from the original biological product.

Understanding the chemistry, manufacturing and controls (CMC) requirements for veterinary pharmaceuticals is essential to support successful registration in the EU.

Master pharmaceutical change control processes in just 1 hour. Learn GxP compliance, change categories, and regulatory requirements for quality professionals.

Learn to conduct thorough audits, identify non-conformities, and recommend corrective actions while following the Golden Rules of successful GMP auditing.

Master pharmaceutical deviation management in just 1 hour. Learn root cause analysis, CAPA processes, and compliance requirements to ensure product quality and safety.

This course covers technology transfer for solid dosage forms, focusing on best practices, strategies, and real-world challenges through interactive sessions and case studies.

A two-day course that will ensure you comply with new regulatory requirements.

During this course, data integrity will be discussed from the perspective of GxP audits, with practical advice for successful data integrity audits given.

Learn how to lead effectively when it matters most. This course provides pharmaceutical managers with an insight into tactical decision-making and the essential skills needed to manage rapidly developing crises.

This course will cover key terminology, the EU and USA regulatory framework, Good Manufacturing Practice (GMP) requirements including controls and validation, and consider Good Distribution Practice (GDP) and how to manage your supply chain.

A two-day event that will provide an invaluable overview of the EU system for variations, with practical advice on the preparation and submission of variation applications using the various European procedures.

This training course prepares professionals in pharmaceuticals, healthcare, and manufacturing to navigate regulatory inspections by major health authorities including the FDA, MHRA, WHO, and EMA.

Master pharmaceutical compliance essentials for storage and distribution. Learn regulatory requirements, best practices, and 3PL supplier optimisation in just 1 hour.

Whether you’re looking to optimise existing processes or lay groundwork for a digital transformation, the course will teach the tools to leverage Digital CMC as a cornerstone of Pharma 4.0 success.

This must-attend event will provide an essential overview of the opportunities and challenges presented by orphan drug regulation.

This course will help delegates gain a better understanding of the software automation technology driving change within the clinical trials landscape.

This comprehensive two-day course will introduce you to the core concepts of what makes an excellent leader - in the context of the pharmaceutical industry - and how to apply the different skills of leading your staff and team to maximise results

One of the most valuable tools for auditors in the pharmaceutical industry is the ability to conduct thorough and effective interviews during audits. This training will equip you with these essential skills.

Linking the technical requirements of device design and pharmaceutical product development. Using QbD to deliver drug/device combinations.

Drive regulatory success with this two-day course for RA and Regulatory Operations professionals. Master practical project management tools, stakeholder strategies, and risk planning through a focused, real-world regulatory case study.

This training will equip attendees with the practical skills necessary to implement regulatory-compliant distribution and storage systems, ensuring both pharmaceutical integrity and patient safety.

Learn how to build digital technology that is specifically aligned to match with the patient, the clinical study, the disease and the treatment programme.

This two-day interactive course covers the essential interpersonal skills needed to excel as a life sciences project manager.

The ability to create a working relationship with your partners in a technology transfer is normally overlooked. In the current pharmaceutical landscape, gaining trust should never be an after thought.

A deep dive into the importance of real world evidence (RWE), real world data (RWD) and artificial intelligence (AI) in pharmaceuticals.

In this course, you will see the value of remote patient adherence monitoring and learn how to stay ahead of the curve by creating your own digital solutions. 

This session will summarise the EU AI Act and its implications on the healthcare sector, including how to be compliant with the new regulatory framework.

Explore the applications and significance of molecular biology in the pharmaceutical industry, covering DNA, RNA, proteins, gene expression, biotechnology, drug discovery, personalised medicine, and the latest breakthroughs like CRISPR-Cas9 and mRNA vaccines.

Master regulatory compliance and material selection as healthcare shifts towards sustainable bioplastics.