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The Center for Professional Innovation & Education

Training for Pharmaceutical, Biotechnology and Medical Device Professionals

As the global leader in accredited biotech, biopharmaceutical, medical device and pharmaceutical training, The Center for Professional Innovation & Education (CfPIE) is proud to offer what we call "Total Learning™". This is the idea that life sciences personnel have unique educational needs that coincide with busy schedules and an ever-changing professional landscape. As such, CfPIE has developed several different ways to help you stay current with industry trends and develop the job skills you need for career advancement:
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Online Training

CfPIE has partnered with ClearPoint Learning Technologies to deliver a truly innovative, best-in-class online learning experience to pharmaceutical, biotech and medical device personnel. By combining CfPIE’s industry-best content with ClearPoint’s award-winning eLearning platforms, we have developed a highly-interactive, personalized approach to learning.
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Classroom Training

For some, there is still no substitute for the classroom experience. Learning through expert knowledge, interactive case studies, workshops, and anecdotally from peers is still the most comprehensive way to absorb information. To help with those needs, CfPIE still offers over 270 public biotech, medical device and pharmaceutical training courses, along with customized client-site training programs each year.
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Blended Learning

Why choose when you can have both? From medical device to pharmaceutical training, CfPIE has designed its online courses to be 100% compatible with the associated classroom training. This blended approach maximizes the absorption of even the most complex materials, and can be had for the same price as a regular classroom course.
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Certification Programs

CfPIE offers nine professional certification programs, which are meant to give pharmaceutical, biotech and medical device personnel the skills and experience they need to advance their careers. Even better, participants can earn this formal credential at no cost above standard course fees!
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From product discovery through commercialization, CfPIE has the training solution to help you advance your career and keep your firm compliant. Listed below are the course topics we offer: At CfPIE, we’re in the business of making employees more valuable and keeping your firm compliant with industry regulations. Register for a biopharmaceutical, medical device, biotech or pharmaceutical training course today. CfPIE provides "results that matter, programs that work and solutions that last."


Upcoming Classroom/Blended Courses
 
May 21 & 22, 2012 FDA Inspections: What Regulators Expect and How to Prepare™
May 21 & 22, 2012 The EU Clinical Trial Directive™
May 21 & 22, 2012 Writing Effective Standard Operating Procedures and Other Process Documents™
May 23 & 24, 2012 Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries™
May 28 & 29, 2012 European Filing & Registration Procedures™
June 04 - 06, 2012 Good Clinical Practices (GCPs)™
June 04 & 05, 2012 Auditing and Qualifying Suppliers and Vendors – An Effective Risk Based Approach™
June 04 & 05, 2012 Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products™
June 04 & 05, 2012 Practical Methods for Project Management™
June 06 & 07, 2012 Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries™
June 07 & 08, 2012 Adverse Drug Events – Reporting & Regulatory Requirements™
June 11 & 12, 2012 Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products™
June 11 & 12, 2012 Clinical Trial Design For Medical Devices™
June 11 & 12, 2012 The Electronic Common Technical Document (eCTD): Building Comprehensive Functionality for Effective Implementation™
June 11 & 12, 2012 Validation of Computer Systems™
June 12 & 13, 2012 FDA Inspections: What Regulators Expect and How to Prepare™
June 13 - 15, 2012 QA/QC Strategy for Biologics and Biopharmaceuticals™
June 13 & 14, 2012 Pediatric Clinical Trial Design - Ethics, Management and Regulatory Requirements™
June 18 & 19, 2012 Preparation of FDA Submissions and Communicating with the FDA (INDs, NDAs, BLAs, ANDAs, ABLAs, Post-Approval Supplements)™
June 20 - 22, 2012 CMC Regulatory Compliance for Biopharmaceuticals and Biologics™
 



Courses by Type I Online Courses I Classroom/Blended Courses by Date I Classroom/Blended Courses by Location I Course Catalog I Certification Programs
On-Site Training I What is "Total Learning™?" I Course Suggestions I Course Locations & Transportation I Accreditation I About Us I Client Endorsements
News & Events I FAQs I Teach for CfPIE! I Course Cancellation Form I Site Map I Cancellation Policy I Discount Policy

The Center for Professional Innovation & Education, Inc. ®
7 Great Valley Parkway, Suite 128
Malvern, PA 19355
Phone: 610-688-1708
©2001 - 2012 CfPIE, Inc. All Rights reserved