Drug Development

Listings
  • Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

    Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

    Drug Development Zurich, Switzerland ( Zurich, Switzerland) November 9, 2017 1695.00 Dollar US$

    Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also kn...

  • Japan Regulatory Compliance Requirements for Life Science Products

    Japan Regulatory Compliance Requirements for Life Science Products

    Drug Development Seattle (Washington) September 5, 2018 1495.00 Dollar US$

    Course "Japan Regulatory Compliance Requirements for Life Science Products" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This 2-Day seminar covers the detai...

  • Drug Master Files and Quality Agreement Training Seminar 2018

    Drug Master Files and Quality Agreement Training Seminar 2018

    Drug Development Philadelphia (PA,PA) March 6, 2018 1495.00 Dollar US$

    Overview: This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, there have been several misunderstandings be...

  • Verification vs Validation-Product, Equipment and QMS Software

    Verification vs Validation-Product, Equipment and QMS Software

    Drug Development Fremont (California) June 15, 2018 290.00 Dollar US$

    Overview: You will learn What do the U.S. FDA and EU Expect for Verification and Validation, Actions and documentation to meet U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements, ISO 14971 and IEC 62366 considerations, as approp...

  • 2017 FDA Data Integrity for Computerized Systems Seminar by  GlobalCompliancePanel

    2017 FDA Data Integrity for Computerized Systems Seminar by GlobalCompliancePanel

    Drug Development Mumbai (India ) February 16, 2017 209.00 Dollar US$

    Overview: The Problem: We have all heard of Data Integrity but do you really understand what it is? Do you understand how 21 CFR 11 and Annex 11 fit into this picture? Specifically, can you answer questions on the following? • Evolution of 21 CFR Par...

  • Expectations for Products Used in Early Phase

    Expectations for Products Used in Early Phase

    Drug Development Fremont (California) March 21, 2018 150.00 Dollar US$

    Overview: This presentation will review the GMP guidance document and discuss how it may be integrated with the recommendations of the guidance documents on CMC requirements. Areas Covered in the Session: Discussion of the elements found in the guida...

  • Compliance for Electronic Records and Signatures 2018

    Compliance for Electronic Records and Signatures 2018

    Drug Development Fremont (California) February 22, 2018 150.00 Dollar US$

    Overview: This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to greatly increase productivity. Areas Covered in the Session: Which data and systems are subject to Part 11 What Part 11 means to...

  • Medical Device Single Audit Program Preparation

    Medical Device Single Audit Program Preparation

    Drug Development Fremont (California) February 22, 2018 150.00 Dollar US$

    Overview: The International Medical Device Regulators Forum (IMDRF) recognizes that a global approach to auditing and monitoring the manufacturing of medical devices could improve their safety and oversight on an international scale. Why should you A...

  • HbA1c ELISA Kit

    HbA1c ELISA Kit

    Drug Development Shirley (New York ) June 28, 2018 10.00 Dollar US$

    Mouse Glycated hemoglobin A1c ELISA Kit kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of the Glycated hemoglobin A1c. This ELISA kit is for research use only, not for therapeutic or diagnostic applications.

  • Cell Banking

    Cell Banking

    Drug Development Shirley (New York) May 30, 2018 1.00 Dollar US$

    Creative Biolabs provides professional cGMP compatible custom cell banking service to clients. Under strict cGMP guideline, both master and working cell banks (MCB and WCB) can be manufactured by experienced cell culture specialists in state-of-the-a...

  • PER.C6 Cell Lines

    PER.C6 Cell Lines

    Drug Development Shirley (New York) May 30, 2018 1.00 Dollar US$

    Creative Biolabs is a pioneer and undisputed global leader in recombinant antibody manufacture and service, we have years of experience in using PER.C6 cell line to produce various recombinant antibodies by both transient and stable transfection expr...

  • Huh-7 Cell Lines

    Huh-7 Cell Lines

    Drug Development Shirley (New York) May 30, 2018 1.00 Dollar US$

    With access to Huh-7 cell line of high quality, various expression vectors with strong promoters as well as other technologies for cell line construction, Creative Biolabs is dedicated to providing customer-oriented cell line services according to yo...