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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

 

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

8th Clinical Quality Oversight Forum: Oct. 11-13 - Philadelphia, PA

5th Promotional Review Committee Compliance & Best Practices: Oct. 16-17 - Florham Park, NJ

4th Technology Transfer for Biologics: Oct. 16-17 - Boston, MA

4th Clinical Trials Phase I & Phase IIA Summit: Oct. 19-20 - Philadelphia, PA

Data Monitoring Committee Optimization Summit: Oct. 19-20 - Philadelphia, PA

2nd Strategic Partnerships for Drug Repurposing Forum: Oct. 26-27 - Boston, MA

2nd Priority Review Voucher Summit: Oct. 26-27 - Boston, MA

Neglected Tropical Diseases Forum: Oct. 26-27 - Boston, MA

10th Partnering with IDNs and ACOs Summit: Nov. 2-3 - Los Angeles, CA

2nd Payer Partnership Forum: Nov. 2-3 - Los Angeles, 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

4th Human Abuse Liability & Abuse-Deterrent Formulations: Nov. 6-7 - Bethesda, MD

Value-Based Strategies for Reimbursement & Formulary Success: Nov. 6-7 - Bethesda, MD 

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

4th Adverse Event Reporting and Safety Strategies Summit: Dec. 4-5 - Philadelphia, PA

2nd New Product Planning Summit: Dec. 7-8 - 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

How to go Paperless in an FDA-Regulated Environment using Electronic Workflow Signature Approvals and Electronic Records
Oct. 3, 2017

eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Oct. 4, 2017

Creating an Effective Contamination Control & Environmental Monitoring Program
Oct. 5, 2017

Why Drug & Dietary Supplement Companies Get Warning Letters: How to Handle and Avoid Them
Oct. 5, 2017

FMEA and Fault Tree Analysis for Preventing Hospital Risks
Oct. 11, 2017

How to Write Procedures to Avoid Human Errors
Oct. 12, 2017

Marketing to Medicare or Medicaid Beneficiaries - What You Can and Cannot Do
Oct. 12, 2017

Understanding ICH Q11FDA's Guidance on the Development and Manufacture of Drug Substances
Oct. 13, 2017

Understanding and Preventing Clean Room Contamination: Gaining and Re-establishing Control of your Cleanroom
Oct. 13, 2017

Using a Learning Management System (LMS) to Develop Pharma Training Curricula
Oct. 18, 2017

How Long Should I Keep My Patients' Medical Records? Disposition of Records and Records Retention for Medical Records, Including Electronic Records
Oct. 18, 2017

How to track gifts to physicians under the Stark Law Non-Monetary Compensation Rule
Oct. 24, 2017

Bioassay Development and Method Validation
Oct. 31, 2017