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  • Guidance on Software and Device Changes and the 510(k)

    Guidance on Software and Device Changes and the 510(k)

    Drug Development Fremont (California) August 14, 2017 Free

    Overview: The first guidance document clarifies key terms and provides insight as to how a risk assessment can help medical device manufacturers to evaluate whether a new 510(k) is required. Why should you Attend: Anyone who is involved in software a...

  • NIST Cybersecurity Framework For Computer Systems Validation

    NIST Cybersecurity Framework For Computer Systems Validation

    Quality Control, Safety & Security Fremont (California) August 14, 2017 Free

    Overview: Computer systems used in highly regulated companies include sensitive and valuable information. Some of this information includes valuable electronic submissions, clinical information, medical device design control records, legal informatio...

  • Batch Record Review and Product Release - 2017

    Batch Record Review and Product Release - 2017

    Drug Development Fremont (California) August 14, 2017 Free

    Overview: A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of pharmaceuticals, biologics, medical devices, etc. Why should you Attend: ...

  • Compliance for Computer Systems Regulated by FDA - 2017

    Compliance for Computer Systems Regulated by FDA - 2017

    Chemical Methods Fremont (California) August 14, 2017 Free

    Overview: The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philo...

  • Laboratory Have an Instrument Calibration Program -2017

    Laboratory Have an Instrument Calibration Program -2017

    Chemical Methods Fremont (California) August 14, 2017 Free

    Overview: This web seminar builds on the terminology found in 21CFR160(b)(4) and introduces terminology and concepts not found in the regulation, but necessary for an effective calibration program, such as instrument classifications. Why should you A...

  • 20th World Congress on Biotechnology and Biotech Industries Meet

    20th World Congress on Biotechnology and Biotech Industries Meet

    Cell Biology & Microbiology London Lakes, TAS (United Kingdom) August 9, 2017 699.00 Dollar US$

    Conference Series LLC extends its warm welcome to Biotech Congress 2018 during March 05-07, 2018 at London, UK with a theme “Future prospects for Biotechnology and Economic Growth”. Conference Series LLC through its Open Access Initiative is committe...

  • Inhalation & Respiratory Drug Delivery USA Congress

    Inhalation & Respiratory Drug Delivery USA Congress

    Drug Development San Diego (California) August 9, 2017 Check with publisher

    Oxford Global Conferences are proud to present our Inhalation & Respiratory Drug Delivery USA Congress, 12 – 13 March 2018, San Diego, USA with our co-located Formulation & Drug Delivery USA Congress. Across the two days, over 200 senior indu...

  • Next-Generation Antibodies and Protein Analysis (2nd edition)

    Next-Generation Antibodies and Protein Analysis (2nd edition)

    Cell Biology & Microbiology Ghent (Ghent) July 18, 2017 Check with publisher

    Next-Generation Antibodies and Protein Analysis (2nd Edition) A VIB TOOLS & TECHNOLOGIES CONFERENCE The Next Generation Antibodies and Protein Analysis: Tools and Technologies meeting (NGAPA) in June 2015 was a great success and we are pleased to...

  • What does Quality mean to you? Quality is not an Organization

    What does Quality mean to you? Quality is not an Organization

    Training and Teaching Fremont (California) July 14, 2017 Free

    Overview: This webinar will help you understand the various interpretations.We will discuss concepts for creating a culture of quality and management excellence with your company. Why should you Attend: Every organization has stakeholders. Your custo...

  • FDA inspectional - Training Practices for FDA Compliance - 2017

    FDA inspectional - Training Practices for FDA Compliance - 2017

    Training and Teaching Fremont (California) July 14, 2017 Free

    Overview: Trainings are either not planned, not conducted, not evaluated or not documented as expected by inspectors. On the other hand it has been is estimated that about 5% of employee's time is spent for training. Areas Covered in the Session: GxP...

  • OOS, Out-Of-Specification Laboratory Results

    OOS, Out-Of-Specification Laboratory Results

    Clinical Fremont (California) July 14, 2017 Free

    Overview: The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory invest...

  • Good Laboratory Practices - Under Analytical Method Validation

    Good Laboratory Practices - Under Analytical Method Validation

    Clinical Fremont (California) July 14, 2017 Free

    Overview: All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more. Why should you Attend: Any laboratory that supports products for sale or use in the United S...