On Demand Webinars

Following is a list of webinars which happened recently. You can choose one or more of the following webinars and we will send you the webinar materials, audio/video so that you can listen/watch at your ease.

How to Make Efficient FDA-Compliant Clinical Protocol Amendments

Regulatory Strategies for Small and Medium Companies

Avoid Data Integrity Issues: How to Audit a CRO and Other Vendors

Trial Master File (TMF): FDA Expectations from Sponsors and Sites

New 510k for Modified 510k-Cleared or 510k-Exempt Devices: Best Practices

Expedited Approval Pathways in the US: Best Ways to Get the Most Incentives

How to write a good Clinical Study Report (CSR) for FDA submission

FDA Rules for Investigating Out-of-Specification (OOS) Test Results

Cleaning Validation for GMP Facilities

CMC Considerations for INDs and NDAs for 505(b)(2) Products

HIPAA Training and Certification for Clinical Trial Professionals: What Applies, What Doesn't

Development and Marketing of Human Cells, Tissues and Cellular and Tissue-Based Products (HCT/Ps) In the US

Social Media and Clinical Trials: Patient-Physician Interactions, Patient-Patient Interactions

Using Excel Spreadsheets in FDA Regulated Environment

Good Documentation Practices for FDA-Regulated Industry

Dispute Resolutions with FDA: Clinical, CMP, and Application Reviews

How to Ace an FDA Meeting

Strategies for 510(k) Applications for Software or Software Containing Medical Devices

Software Validation: Avoiding FDA Warning Letters and Consent Decree

Is Your Facility Validated for cGMP? 5 Steps to Compliance with FDA

How to Use FDA's Guidance Documents To Your Advantage

How to Apply for a Breakthrough Therapy Designation and Win It

FDA IND Submission for a Product

Cybersecurity and FDA: Navigating FDA Rules for Cybersecurity in Regulated Products

How to Increase the Odds for Success of Your 505(b)(2) Product

5 Steps to Finding the Best Sites for Your Clinical Trial

Strategies for Minimizing Preclinical Testing: Meeting FDA Requirements without Breaking the Bank

FDA Compliant Warehouse and Distribution Practices

FDA Regulation of Molecular Diagnostics

FDA Policies and Expectations For Developing Companion Diagnostics

Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials

How to Start a New Clinic as a Trial Site

Adverse Event Reporting Requirements for Dietary Supplements and OTC Drugs

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On Demand Webinars

For more info, fill the box below. We will contact you within 24 hrs.

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