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62 results of "Life Sciences x" and "Biotech & Biologics x"
On-Demand Webinar

Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach

The various regulatory agencies have expectations that suppliers and vendors will demonstrate control over their manufacturing processes, validations, and documentation. Quality auditing is the process of checking whether these organizations have implemented w ...

Recorded Webinar

Medical Device Complaints & CAPA

This webinar will explain the CAPA process from information gathering through MDR and Recall decision making to final CAPA closing. Post closing effectiveness evaluation is required and will be explained. Preventative Action is often neglected and will be disc ...

Recorded Webinar

Practical Implementation of Pharmaceutical Quality Risk Management (QRM)

Recognize the purpose and value of Quality Risk Management (QRM), as well as how it applies to your job Explain the level of risk based on severity, occurrence, and detectability and how the QRM process is used to make decisions Identify key QRM terminolog ...

Recorded Webinar

Post marketing responsibilities for pharmacovigilance in the European Union (EU)

There is comprehensive regulation around the safety of medicines in the EU and marketing authorization holders have extensive responsibilities in this area for the drugs they market. The presentation will provide information on the requirements for pharmacov ...

Recorded Webinar

Effective Batch Record Review

In this webinar attendees will learn the fundamentals for reviewing batch records in a pharmaceuticals, biologics and medical devices environment. You will hear about the proper training that must be demonstrated before one is considered a suitable reviewer of ...

On-Demand Webinar

Cannabinoids as Drugs

This webinar will discuss the current status of cannabinoids as medical products in the United States. The focus will be on what we can learn from the FDA approval of Epidolex (Cannabidiol) oral solution 100 mg/mL. How to obtain research information will be pr ...

Recorded Webinar

Technical Writing: A Detailed Process

Provides step-by-step instructions to produce excellent written presentations Learn how to balance between being precise enough to cover the subject matter yet general enough to apply to other locations and/or projects Learn how to deal with reviewers and ...

Recorded Webinar

Technical Writing Training

Provides in-depth training in a highly specialized field Learn strategies that can be applied such that this training is not overwhelming Train Technical Writers in general guidelines for the creation and maintenance of documents Training for Technical Wr ...

Recorded Webinar

Assessment of Drug Interactions in Drug Development

Drug-drug interactions are a common problem and result in hospital admissions for medically important and even fatal adverse events. Drug-drug interactions can also cause partial or complete abolishment of treatment efficacy. The ageing population, where p ...

Recorded Webinar

21 CFR 111 GMP Dietary Supplement Laboratory

This training program will provide an overview of 21 CFR 111 regulatory requirements which governs how dietary supplements are manufactured and tested It will futher review the test procedures and documentation requirements to ensure regulatory compliance ...