Life Sciences

Listings
  • Is My Nanotechnology Safe? Approaches For NanoEHS Risk Assessments

    Is My Nanotechnology Safe? Approaches For NanoEHS Risk Assessments

    Life Sciences san Jose (california) April 17, 2021 Check with publisher

    The FDA is still treating nanomaterials on a case by case basis. How can you determine if the nanotechnology you are considering is safe? FDA applications require proof of safety, as does public perception in an environment where using nanomaterials ...

  • Batch Record Review and Product Release

    Batch Record Review and Product Release

    Life Sciences san Jose (california) January 31, 2021 Check with publisher

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

  • SaaS/Cloud Risk-Based Validation With Time-Saving Templates

    SaaS/Cloud Risk-Based Validation With Time-Saving Templates

    Life Sciences san Jose (california) January 31, 2021 Check with publisher

    This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud hosted applications. It explains how to write a Data Privacy Statement for compliance with EU General Data Protecti...

  • Analytical Instrument Qualification and System Validation

    Analytical Instrument Qualification and System Validation

    Life Sciences san Jose (california) January 30, 2021 Check with publisher

    Analytical equipment should be qualified, and computer systems should be validated to demonstrate suitability for their intended use. To be acceptable to regulatory authorities, electronic records must comply with 21 CFR Part 11, Annex 11 to EU GMPs ...

  • The Drug Development Process from Concept to Market

    The Drug Development Process from Concept to Market

    Life Sciences san Jose (california) January 30, 2021 Check with publisher

    This course is designed to cater for employees of pharmaceutical companies who would like an understanding of the drug development and regulatory approval process. The course starts by considering the global pharmaceutical market, important therapeut...

  • Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact

    Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact

    Life Sciences san Jose (california) December 18, 2020 Check with publisher

    The course will cover the factors used by the FDA to schedule inspections. You will learn how to predict what an FDA investigator will do and what they will cover in the inspection. There should be no surprises if you have prepared properly. Firms ne...

  • Cannabis Formulation/Product Development Strategies for Medical/Recreational Oral Dosage Forms

    Cannabis Formulation/Product Development Strategies for Medical/Recreational Oral Dosage Forms

    Life Sciences san Jose (california) December 12, 2020 Check with publisher

    Successful cannabis product development requires having the-end-in-mind regarding excipients-cannabinoids compatibility, shelf-life/product stability and bioavailability of cannabinoids. This webinar will utilize presenter’s expertise and experience ...

  • Quality Control Laboratory Compliance - cGMPs and GLPs

    Quality Control Laboratory Compliance - cGMPs and GLPs

    Life Sciences san Jose (california) November 28, 2020 Check with publisher

    FDA inspection and oversight of quality control (QC) laboratories are essential elements of the agency’s evaluation of the compliance status of regulated companies representing multiple industries - pharmaceuticals, biologics, medical devices, as wel...