Food, Drugs, Biologics

Compliance Trainings will provide insight into various aspects of Food Compliance like prescription drugs, including testing, manufacturing, labeling, advertising, marketing, efficacy and dietary supplements through industry experts.
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Webinar On 21 CFR 11 Compliance for Excel Spreadsheets Spreadsheet Applications such as MS Excel are frequently used in 21 CFR 11 compliant environments, but they were not specifically designed for regulated environments and their development is not optimized for 21 CFR 11 compliance  For more information about this event please visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1399

Webinar On How to select Software for a Regulated Environment Scheduled On : Monday, March 2014 at Hrs Duration : 120 Minutes

Webinar On Annual Reports for Approved PMAs  Scheduled On Thursday, December 11, 2014 at 13:00 Hrs  This webinar describes the information required by FDA to be submitted in a PMA annual report. The webinar also discusses FDA recommendations for level of detail the applicant should provide in the PMA annual report.  For more information visit  https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1402

Webinar On Annual Reports for Approved PMAs Scheduled On Thursday, December 11, 2014 at 13:00 Hrs This webinar describes the information required by FDA to be submitted in a PMA annual report. The webinar also discusses FDA recommendations for level of detail the applicant should provide in the PMA annual report. For more information visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1402

Webinar On 21 CFR 11 Compliance for Excel Spreadsheets Scheduled On Tuesday, October 21, 2014 at 13:00 Hrs presenting by Angela Bazigos.  Spreadsheet Applications such as MS Excel are frequently used in 21 CFR 11 compliant environments, but they were not specifically designed for regulated environments and their development is not optimized for 21 CFR 11 compliance  For more information visit  https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1392

Webinar On How to select Software for a Regulated Environment Scheduled On : Monday, March 2014 at Hrs Duration : 120 Minutes

Webinar On Statistical Analysis of Gages Scheduled On Friday, September 25, 2014 at 13:00 Hrs  The seminar begins with an examination of the fundamental vocabulary and concepts related to metrology. Topics include: accuracy, precision, calibration, and "uncertainty ratios".   For more information visit  https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1272

Webinar On Statistical Analysis of Gages Scheduled On Friday, September 25, 2014 at 13:00 Hrs The seminar begins with an examination of the fundamental vocabulary and concepts related to metrology. Topics include: accuracy, precision, calibration, and "uncertainty ratios". For more information visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1272

Webinar On Current GMP Requirements for Combination Products - Final Rule Scheduled On :  Thursday, September 4, 2014 at 13:00 Hrs  This webinar discusses this final rule and describes approaches to comply. At the end of this session, you will be able To understand where the combination products GMP rule applies.   For more information visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1062

Webinar On -ICH Pharmaceutical Quality System Scheduled On : Wednesday, February 2014 at Hrs

Webinar On Webinar on Proactive #Internal #Auditing-The Key to Establishing, Maintaining, and Improving Quality Systems  This webinar provides a broad overview of the internal auditing functions starting with the concept of quality systems and their objectives, primarily using graphical methods.   For more information visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1065

Webinar On -ICH Pharmaceutical Quality System Scheduled On : Wednesday, February 2014 at Hrs

Webinar On FDA Regulation of Mobile Apps Scheduled On Monday, September 22, 2014 at 13:00 Hrs. The use of mobile apps as a medical device continues to mushroom. Approximately 85% of adults use cell phones. They offer a fertile field for mobile apps used for medical purposes, some good, some not.  https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1127

Webinar On Managing the FDA form Inspection Observations will be held on Tuesday, March 2014 at Hrs Duration : 60 Minutes FDA medical device Food and Drugs Administration Pharma Regulatory compliance

Webinar On Patient Compliance in Drug Trials Scheduled On Thursday, August 7 , 2014 at 13:00 Hrs.  This 1 hour virtual seminar will help you understand compliant issues researchers face while conducting clinical trials especially in the drug trials.  For more information visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1321

Webinar On Patient Compliance in Drug Trials Scheduled On Thursday, August 7 , 2014 at 13:00 Hrs. This 1 hour virtual seminar will help you understand compliant issues researchers face while conducting clinical trials especially in the drug trials. For more information visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1321

Webinar On Managing Product and Process Risk through Failure Mode and Effects Analysis (FMEA) Scheduled On : Wednesday, April 29, 2015 at 13:00 Hrs For more information about this event please visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1244

This FDA GMP training will help you understand the current requirements for raw material management with tips for practical implementation.

Many laboratories are unsure about which QC practices are needed to assess media performance to meet not only their requirements, but also the requirements of ISO/IEC 17025: 2005. In this webinar Mr. Michael Brodsky will discuss a practical QC approach for in-house prepared and/or commercially purchased media and reagents specifically applicable to microbiology laboratories. Don’t miss this valuable training Last date will be sign up is Scheduled On : Sunday, July 12, 2015

Designing software solutions for companies doing business in regulatory environments to move products to market faster, while reducing costs.

This webinar should be "required reading" for those who want to be a member of a drug project team and any of the sub-teams. The first step in the drug development approval process is knowing what needs to be done.

Is it Method Verification or Validation, or Just Semantics? This Webinar will discuss the distinction between and requirements for method validation and method verification, to comply with ISO/IEC Standard for a microbiology laboratory.

Webinar On Managing the FDA form Inspection Observations will be held on Tuesday, March 2014 at Hrs Duration : 60 Minutes FDA medical device Food and Drugs Administration Pharma Regulatory compliance

Webinar On Transfer of Analytical Methods and Procedures according to USP 1224 Scheduled On : Wednesday, April 22, 2015 at 13:00 Hrs This seminar will give a good understanding of USP and FDA requirements and provide recommendations and tools for effective implementation. For more information about this event please visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1453

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