US Pharmaceutical vs Device Clinical Development Similarities and Differences Explored

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					 Live Webinar on : US Pharmaceutical vs Device Clinical Development: Similarities and
 Differences Explored
 Thursday, June 28, 2012duration    : 02:00 to 03:00 PM EDT

                                              Why should you attend :

                                               In the US, clinical development of both devices and
                                              drugs are regulated by the FDA. While there are
                                              many similarities between regulatory requirements
                                              for the two types of products, there are also some
                                              important differences.

Get 15 % Discount as a early bird             - List at least three differences between the clinical
registrations. Use Promo Key :                development and approval of drugs versus devices
                                              in the US.
                                              -Identify the US regulations that apply to both drug
                                              and device studies.

                                              - Recognize differing product development and
                                              product reimbursement practices of drugs and

                                             Areas      Covered       in    the     Session:      
                                              We will review some key differences between the
                                              pharmaceutical and device industries, regulatory
Live ( Single registration ) : $189.00        requirements common to drug and device clinical studies
Group ( Max 10 Attendee): $249.00             and illustrate some important differences such as
On Demand (Recording available):$289          reimbursement issues specific to device trials.
Get Training CD : $449
Play back(Unlimited views):-309
                                              .About Speaker
Who will benefit: (Titles)

    - Clinical research manages    Glenda Guest is Vice President of Norwich Clinical
- Project managers                  Research Associates Ltd. (NCRA), a full service Clinical
- Clinical research associates      Contract Research Organization (CRO) located in central
- Monitors                          NY State, USA. She has been involved in regulated
- Quality assurance professionals   research since 1997 and specializes in medical device
- Research coordinators             monitoring and project management; GCP, vendor and
- Clinical investigators            third party auditing as well as training on US regulated
                                    research and Good Clinical Practice.


                                    Ms. Guest is an active member of the Association of
                                    Clinical Research Professionals (ACRP) and is a regular
                                    speaker at their local events and global conferences. She
                                    has also presented at a number of other industry-related
                                    events and enjoys sharing her expertise with colleagues
                                    in the clinical research arena.

                                    Ms. Guest has maintained her status as an ACRP Certified
                                    Clinical Research Associate since April of 2002. She is also
                                    recognized by the Society of Quality Assurance as a
                                    Registered Quality Assurance Professional - Good Clinical
                                    Practices (RQAP-GCP),having successfully passed the first
                                    exam for this designation offered by SQA in April 2007.
                      Compliance2go |
                      Phone : 877.782.4696 | Fax : 281-971-0286
                        Email :

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