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 Conferences & Online Training




Conference Registration

 


To Register Online click on a link below
or
Call: 201-871-0474  Fax: 253-663-7224

 

On-Site Conferences

 

Healthcare Ad-Tech and Programmatic Strategy Summit: Aug. 7-8 - Philadelphia, PA

Disclosure and Transparency for Clinical Data Summit: Aug. 7-8 - Philadelphia, PA

6th Clinical Trials Inspection Readiness Summit: Aug. 7-8 - Philadelphia, PA

Life Science Investor Relations Forum: Sep. 7-8 Boston, MA

Validation, Verification and Transfer of Analytical Methods: Sep. 14-15 - Boston, MA

Analytical Instrument Qualification and System Validation: Sep. 14-15 - Boston, MA

Safety Labeling and Packaging Summit: Sep. 14-15 - Florham Park, NJ

Biosimilar Market Access and Commercialization Strategies Summit: Sep.18-19 - Boston, MA

Artificial Intelligence Innovation Summit: Sept 18-19 - San Francisco, CA

2nd Drug Development Forum: Sept 25-27 - Boston MA

FDA's New Import Program for 2017: Oct. 5-6 - San Francisco, CA

Computer System Validation - Reduce Costs and Avoid 483s: Nov. 2-3 - San Francisco, CA

21 CFR Part 11 Compliance for SaaS/Cloud Applications: Nov. 2-3 - San Francisco, CA

Compliance with Advertising and Promotional Requirements: Nov. 9-10 - Boston, MA

 

Online Training


* 60-90 minute seminar (Travel-Free) delivered over the phone and internet.
* Unlimited listeners per connection - bring the entire department.
* Continuing education credits available for most teleconferences

CMS Restraint and Seclusion: Navigating the Most Problematic of all of the CMS Hospital Standards and Proposed Changes
Aug. 2, 2017

How FDA Trains its Inspectors to Review CAPA, and Best Practices for Inspection Preparation
Aug. 3, 2017

21 CFR Part 11 and Annex 11 Compliance - Specifics Needed to Eliminate 483s
Aug. 3, 2017

Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries
Aug. 8, 2017

Annual Current Good Clinical Practices (cGCP) Training
Aug. 9, 2017

Qualification of the Dissolution Apparatus
Aug. 9, 2017

Acceptance Activities in FDA QSR
Aug. 10, 2017

Medical Device Software Verification and Validation
Aug. 10, 2017

Documentation of Medical Necessity - Focus for OIG and other auditors
Aug. 10, 2017

Latin America - Understanding Regulatory Compliance Requirements Across the Life Science Industry
Aug. 14, 2017

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Aug. 15, 2017

Supplier Quality Agreements - Essential for Suppliers of Many Outsourced Processes
Aug. 16, 2017

Processes & Effects of Immunogenicity to Biologics & the Screening Methodologies - 3 hour Virtual Training
Aug. 16, 2017

The Use of Monitoring and Statistics to Prevent Non-Compliance in the Laboratory
Aug. 16, 2017

Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements
Aug. 17, 2017

FDA's Ambitious Regulation of Social Media
Aug. 22, 2017

Care of the LGBT Patient and Their Families: Policies, Procedures & Practices to Ensure Quality Care and Reduce Liability
Aug. 22, 2017

Medical Record: Compliance with CMS Hospital CoPs and Proposed Changes
Aug. 22, 2017

The New Usability Engineering Requirements of IEC 62366-1:2015, 2: 2016
Aug. 23, 2017

Interdisciplinary Care Rounds: A Key Strategy for Improving Case Management Outcomes
Aug. 23, 2017

Data Integrity in the Pharmaceutical Laboratory: Practical Steps to Identify and Avoid Data Integrity Issues
Aug. 23, 2017

Objectionable Microorganisms in Biopharmaceutical Manufacturing
Aug. 24, 2017

Understanding and Implementing USP <1058>: Analytical Instrument Qualification
Aug. 30, 2017