Pharmaceutical Certificate courses

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Current Good Manufacturing Practice (cGMP)

cGMP Training for Employees

Good Laboratory Practice (G(QC)LP)

Validation for Pharmaceutical Manufacturing

Good Clinical Practice (GCP)

Clinical Research Monitoring

Drug Safety and Pharmacovigilance

Pharmaceutical Regulatory Affairs

Medical Device Regulatory Affairs

Medical Devices

IT/IS for Biopharma

21 CFR Part 11

21 CFR Part 211

21 CFR Part 820

Pharmaceutical compliance training is a must in the ever-changing world of pharmaceuticals.

As new pharmaceuticals are developed, the laws and regulations regarding their production, distribution, and sales are constantly changing. This means that pharmaceutical professionals must stay abreast of all of the latest developments and changes to pharmaceutical law and practice. In addition, pharmaceutical companies must keep abreast of the FDA's constant inspection of their plants and manufacturing areas.

Pharmaceutical compliance training not only ensures employees receive proper education about new regulations and laws, it also prepares them for various industry-related emergencies.

World Compliance Seminars (WCS) understands this ever changing training requirement of the Pharma industry and thus designs and delivers course in the form of webinars, seminars and on site training.By staying on top of changes in the regulations governing the pharmaceutical industry, you will help to protect your business interests and promote your company.It is not enough for pharmaceuticals companies to simply rely on the knowledge and skills of their employees.

New pharmaceuticals are being developed every year, and the new regulations and laws related to those products and drugs can change the way that a company produces and distributes its products year after year. Manufacturers are often required to conduct certain manufacturing processes,audits that involve the use of dangerous chemicals. While many chemical products are used in good manufacturing practices, there is always the possibility that an unsafe chemical or substance has been used in the process.

Pharmaceutical Training and Continuing Education

By receiving proper training in pharmaceutical formulation, pharmaceutical transfer processes , GLP, GMP, Clinical Compliance, Process Validation, Global Regulatory Affairs, Document Management, GMP (Good manufacturing practice) QSR and CMC hazardous drugs, you can ensure your staff receives proper hazard recognition and adequate protection from these harmful products.

Another reason pharmaceutical companies must undergo continual training is to make sure they are compliant with all of the mandatory reporting requirements of the Food and Drug Administration (FDA) and avoid warning letters (483s). According to FDA reports, pharmaceuticals require the testing of their products for contamination, effectiveness, and safety on a regular basis. Pharmaceutical compliance training helps ensure your company is regularly submitting reports to the FDA.

WCS offers both online and classroom courses. It is important to consider what your needs are when considering either option. Online courses typically allow you to work at your own pace, whereas in a classroom situation, you have the lecturers and professors to whom you must report. In addition to the convenience factor of taking your courses at home, you can also schedule course times that coincide with your workday.

Finding the right training provider will make sure that your staff stays up to date on the latest regulations and procedures.

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