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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

 

3rd Payer Partnership Forum - Jun. 11-12 - Boston, MA

ExL Pharma 9th KOL Thought Leadership and Engagement Summit - Jun. 11-12 - Philadelphia, PA

Exl Pharma 9th Aggregate Spend and Open Payments Conference - Jun. 11-12 - Philadelphia, PA

Exl Pharma 9th Digital Pharma West - Jun. 11-13 - S. San Francisco, CA

ExL Pharma ai Innovations for Life Science and Healthcare Summit - Jun. 13-14 - Philadelphia, PA

ExL Pharma 2nd eRegulatory Submissions - Jul. 12-13 - Philadelphia, PA

 

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

Process Capability for Normal and Non-Normal Data
Jun. 11, 2018

Bonified CAPA investigations
Jun. 13, 2018

Medical Device Compliance with MEDDEV 2.7.1 Rev 4 for Clinical Evaluation/CER Reporting
Jun. 13, 2018

Through the Eyes of an Auditor
Jun. 14, 2018

System Suitability Testing (SST) for USP and FDA Compliance
Jun. 14, 2018

Stability Programs for Leachable Impurities
Jun. 19, 2018

Drafting a Software Verification and Validation Report Package and Protocol - The 11 Must-have Documents
Jun. 19, 2018

Medicare’s New Market-Based Reimbursement System for Clinical Laboratory Testing: Tipping Point Ahead for U.S. Labs in 2018
Jun. 20, 2018

Process Validation - Overview of Why and How
Jun. 20, 2018

Approaching unknown cause laboratory investigations using lean tools
Jun. 21, 2018

System Suitability Testing in the Pharmaceutical Laboratory: Addressing FDA and USP Compliance
Jun. 21, 2018

Good Documentation Practices to Support FDA Computer System Validation and Compliance
Jun. 22, 2018

Why and How - Verification of Compendial Methods - USP <1226>
Jun. 27, 2018

Ligature Risks: Ensuring Compliance with the CMS Hospital CoPs and TJC Requirements
Jun. 28, 2018

Understanding FDA Design Verification and Validation Requirements for Medical Devices
Jun. 29, 2018

21 CFR Part 11 - Electronic record and Signature Validation
Jul. 11, 2018

Good Documentation Guideline (Chapter <1029> USP)
Jul. 19, 2018