Available Courses

Results (48)




Course Title Course Date Location
Computer System Validation | Compliance Courses Aug 14, 2017 - Aug 15, 2017 Malvern, PA United States
Clinical Document Management: A Trial-by-Trial Compliance Approach Aug 21, 2017 - Aug 22, 2017 Malvern, PA United States
Clinical Trial Project Management, Phase 1-4 Best Practices Aug 23, 2017 - Aug 25, 2017 Malvern, PA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Sep 11, 2017 - Sep 12, 2017 Malvern, PA United States
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer Sep 11, 2017 - Sep 12, 2017 Malvern, PA United States
Project Management for Medical Device Product Development Sep 11, 2017 - Sep 12, 2017 Malvern, PA United States
Introduction to Medical Combination Products Sep 13, 2017 - Sep 15, 2017 Malvern, PA United States
Process Validation for Drugs and Biologics Sep 13, 2017 - Sep 14, 2017 Malvern, PA United States
Pharmaceutical Production Batch Record Review | Training Sep 14, 2017 - Sep 15, 2017 Malvern, PA United States
FDA Inspections - What Regulators Expect and How to Prepare Sep 18, 2017 - Sep 19, 2017 Malvern, PA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Sep 20, 2017 - Sep 22, 2017 Malvern, PA United States
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Oct 02, 2017 - Oct 03, 2017 Malvern, PA United States
Regulated Medical Marijuana Business - Concept to Product Sale Oct 04, 2017 - Oct 05, 2017 Malvern, PA United States
Introduction to Molecular Biology Techniques Oct 11, 2017 - Oct 13, 2017 Malvern, PA United States
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Oct 12, 2017 - Oct 13, 2017 Malvern, PA United States
Advanced Topics in Biostatistics for Non-Statisticians™ Oct 16, 2017 - Oct 17, 2017 Malvern, PA United States
Preparation of FDA Submissions and Communicating with the FDA Oct 16, 2017 - Oct 17, 2017 Malvern, PA United States
Effective Document Management for Pharma, Biotech & Medical Device Oct 17, 2017 - Oct 18, 2017 Malvern, PA United States
Biostatistics for Non-Statisticians Oct 18, 2017 - Oct 20, 2017 Malvern, PA United States
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Oct 18, 2017 - Oct 20, 2017 Malvern, PA United States
Selecting and Managing CROs Oct 19, 2017 - Oct 20, 2017 Malvern, PA United States
Stability Programs for Determining Product Shelf Life Oct 23, 2017 - Oct 24, 2017 Malvern, PA United States
Writing Effective SOP and Other Process Documents Oct 23, 2017 - Oct 24, 2017 Malvern, PA United States
Marketing and Advertising of Pharmaceuticals & Medical Devices Oct 24, 2017 - Oct 25, 2017 Malvern, PA United States
QA/QC Strategy for Biologics and Biopharmaceuticals Oct 25, 2017 - Oct 27, 2017 Malvern, PA United States
Writing in the Regulated Environment When English Is Your Second Language Oct 25, 2017 - Oct 26, 2017 Malvern, PA United States
Auditing for Medical Devices: ISO 19011:2011 Framework Oct 30, 2017 - Nov 01, 2017 Malvern, PA United States
Auditing for Medical Devices: EN ISO 13485:2016 Changes Nov 01, 2017 - Nov 03, 2017 Malvern, PA United States
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Nov 01, 2017 - Nov 02, 2017 Malvern, PA United States
Lyophilization Technology-Application of Scientific Principles Nov 02, 2017 - Nov 03, 2017 Malvern, PA United States
Auditing and Qualifying Suppliers and Vendors™ Nov 06, 2017 - Nov 07, 2017 Malvern, PA United States
Introduction to Effective Medical Writing Nov 06, 2017 - Nov 07, 2017 Malvern, PA United States
Overview of FDA Regulatory Compliance for Medical Devices Nov 06, 2017 - Nov 07, 2017 Malvern, PA United States
Clinical Trial Design For Medical Devices™ Nov 08, 2017 - Nov 09, 2017 Malvern, PA United States
Medical Writing for Pharma, Biotech and Med Devices Nov 08, 2017 - Nov 10, 2017 Malvern, PA United States
Cleanroom Microbiology for the Non-Microbiologist Nov 13, 2017 - Nov 14, 2017 Malvern, PA United States
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Nov 13, 2017 - Nov 14, 2017 Malvern, PA United States
Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements Nov 15, 2017 - Nov 17, 2017 Malvern, PA United States
Understanding Sterilization Methods for Products and Devices Nov 15, 2017 - Nov 16, 2017 Malvern, PA United States
Design Control for Medical Device Professionals Nov 28, 2017 - Nov 29, 2017 Malvern, PA United States
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Nov 30, 2017 - Dec 01, 2017 Malvern, PA United States
Product Quality Reviews Nov 30, 2017 - Dec 01, 2017 Malvern, PA United States
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Dec 04, 2017 - Dec 06, 2017 Malvern, PA United States
Good Manufacturing Practices Training | GMP Course Dec 04, 2017 - Dec 06, 2017 Malvern, PA United States
Water Purification Systems for Regulated Industries Dec 04, 2017 - Dec 05, 2017 Malvern, PA United States
Heating, Ventilation and A/C in a Regulated Environment Dec 06, 2017 - Dec 08, 2017 Malvern, PA United States
Understanding & Implementing New EU Clinical Trial Regulation Dec 11, 2017 - Dec 12, 2017 Malvern, PA United States
The Drug Development Process from Concept to Market Dec 13, 2017 - Dec 15, 2017 Malvern, PA United States