I'm a SAS programmer of 10 years and am looking to get into clinical trials. can any of you share any insights on the major differences between the 2 and the challenges i may face in transitioning from one to the other.
ALso, does anybody know of any good training programs especially in the bay area? Any suggestions/ideas will be greatly appreciated, Thanks.
You may be interested in my new and unique class, Best Practices in SAS Statistical Programming for Regulatory Submission. It will be a two-day intense and comprehensive class in New Brunswick, New Jersey. During these two days, I expect to review all the details in the submission process and SAS macros for validating and producing publication-quality summary tables. I will also be available to answer any questions you may have.
Best Practices in SAS Statistical Programming for Regulatory Submission
- Download Class Outline and Brochure:
- More update to date information on Class:
- Best Practices in SAS Class Description:
This course is intended for anyone directly or indirectly responsible for
the creation, content or validation of summary tables, data lists and
graphs used to support research, drug or medical device efficacy and
safety in a regulatory submission. Professionals in the pharmaceutical,
biotechnology and medical device industries who want to be 21 CFR Part 11
compliant in relation to the SAS programming environment will benefit from
this unique course. Effective and practical solutions to address real-
world issues will be provided.
This class is offered through The Center for Professional Advancement, an
organization which is CEU accredited.