Top Pharmaceutical and Medical Device Trainings in 2021

Medical Device Directive (MDD) to Medical Device Regulation (MDR) Transition Training Course Online

06-28 Apr Virtual Training Online on EU-MDR to align your company with the new requirements of the Medical Device Regulation (EU-MDR) by UK top Industry Expert

Frank Stein

Frank Stein

€1.695

FDA’s Plan for Modernizing the 510(k) Pathway

20 April This FDA Training online will explain Basic of US FDA’s Expectations for the 510(k), The Medical Device Safety Action Plan and 510(k)

John E Lincoln

John E Lincoln

$179

Vaccine Patents in the Current Pandemic Climate Live Webinar

21 Apr This presentation will discuss not only the global patenting issues facing vaccines but will also look at some of the challenges facing vaccine patenting

Joanna Brougher

Joanna Brougher

$199

Hypothesis Testing, p-values, and Inference: When Thinking Like a Statistician Makes Sense

22 April You will learn the why and how of the scientific method, and how to view the world with a statistician’s eyes

Elaine Eisenbeisz

Elaine Eisenbeisz

$1,025

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Virtual Training

April 20-21-The objective of this FIVE HOUR/DAY, ON-LINE two day interactive seminar is to explore raw materials and their requirements – issues and solutions.

Barry A. Friedman

Barry A. Friedman

$1,295

FDA Computer System Validation ( CSV) Training 3 Days Virtual Seminar

On April 27-29 this Course will explain how to comply with key FDA and international CSV regulations and guidance, such as 21 CFR Part 11 and Annex 11.

Carolyn Troiano

Carolyn Troiano

$1,495

The Veterinary Drug Approval Process and FDA Regulatory Oversight

April 22-23 -This two-day seminar will provide attendees with an understanding of FDA’s veterinary drug approval process, obtaining federal government approval.

Karl M. Nobert

Karl M. Nobert

$1,899

Knock, knock, who’s there? Are you ready for an FDA inspection in the COVID-19 Era and Beyond?

27 April This webinar will help you manage inspections efficiently and effectively. You’ll learn about the FDA’s inspectional approach, focus areas and prepare

Susanne Manz

Susanne Manz

$389

How FDA trains its investigators to review CAPA and what should you do to prepare

28 Apr This webinar will discuss all the documents used by FDA to train their inspectors to review your CAPA system, some of which you may not be familiar with.

Jeff Kasoff

Jeff Kasoff

$199

Our Participants Testimonial


The presentation by Carolyn Troiana today was fantastic, both I and the QA Manager (Aaron Neighbour) loved it and had extensive conversation afterward about it. ( FDA Compliance and Mobile Applications Webinar )

Robert Friedland ( IT Manager) NUTEK BRAVO, LLC.

Thank you for providing the information in such detail. It was helpful to gain the perspective of somebody that has implemented these regulations in a working lab. Virtual Seminar on ( Training on Life cycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines )

Tracey Kessler ( Director of R&D) CEL-SCI Corporation

I felt the seminar was very helpful and provided good insight for DataIntegrity and what the FDA is looking for per the regulations. ( Current Regulatory Thinking on Data Integrity 2 Days Virtual Seminar )

Margaret A. Clifton ( Manager, Quality Systems) CSL Plasma

The presenters subject matter knowledge is extensive which enables information to be shared in detail. (Training Attended on Risk Based Verification and Validation Planning to Meed US FDA and ISO 13485 Requirements )

Stuart Chisholm (Sr. Principal Device Engineer) Teva Pharmaceuticals

About World Compliance Seminars (WCS)

World Compliance Seminars (WCS) is one stop solution for all your pharmaceutical, biotechnology and medical device certification program needs. The pharmaceutical and medical device training requirements are set forth by the FDA (Food and Drug Administration) and other major regulatory bodies like NIH, EMA, as well as numerous European based national regulatory bodies.

These requirements are important to the training of pharmaceutical reps who are responsible for the education, professional development, and on-the-job training. The training is broken down into different sections to cover a wide variety of topics, including pharmaceutical formulation, pharmaceutical transfer processes , GLP, GMP, Clinical Compliance, Process Validation, Global Regulatory Affairs, Document Management,GMP (Good manufacturing practice) QSR and CMC and many more.

The pharmaceutical and medical device requirements that the FDA has set forth are designed to protect the public's health and safety. Pharmaceutical reps must adhere to all of the regulations and education courses provided by the FDA in order to be considered one of the best in their field. They also must complete ongoing educational opportunities and maintenance programs in order to maintain relevance and career enhancement.

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