Health Research, Professional Training

In this course, you will be introduced to basic statistics and study designs used in CER/PCOR and the ethical considerations...

This course provides instruction on the Biocidal Products Regulation (BPR) and its implications on the current and future biocide industry...

The module will cover a range of more advanced methods of demographic analysis, including multiple decrement life tables, health expectancies,...

Global regulatory agencies are committed to implemeting the eCTD as benchmark.  Attending this practical two-day training course by PTI, pharma...

The US is the largest market for pharmaceutical and biotech products making it a key strategic goal for organisations. In...

This course aims to provide students with critical, higher-order skills in order to find, read, appraise and interpret relevant, reliable...

In-vitro in-vivo correlation is a critical tool described in many guidelines and its usage in development is recommended to reduce...

A successful, cost-effective and compliant process can be difficult to achieve. With the latest guidances promoting a lifecycle approach to...

Has your paperwork grown organically over the years? Have you added extra checks, extra fields and immense numbers of signatures...

Accurate and clear strategies for the monitoring of outsourced clinical trials has become more important than ever due to the...

This course will provide attendees with a concise but comprehensive overview of all relevant regulatory, technical and quality elements necessary...

The new Medical Device Regulation, published in 2017 and due to be fully implemented in 2020, will result in significant...

The second course in the online biopharmaceutical and biosimilar CMC analytical series follows on from the first course on regulatory...

Managing regulatory change forfilingvariationsis a complex and challenging procedure. The regulatory requirements highlight the need for successfulvariationsstrategies across regulatory teams....

The newly finalised Medical Device Regulation will mean significant changes to clinical evidence with more clinical data being required for...

The course comprises a series of presentations and workshops, supplemented with distance learning activities. You’ll cover: GCP/GMP legislation (including preparation...

Explore the technical challenges to designing and executing specific critical analytical studies with renowned expert Dr. Nadine Ritter. Practical examples...

This two-day refresher and reassessment programme is specifically designed for you if you’re required to take the formal assessment of...

This is a five-day CPD course which will be delivered with presentations, group discussions and practical sessions illustrating the principles...

Explore the technical challenges to designing and executing specific critical analytical studies with renowned expert Dr. Nadine Ritter. Practical examples...