Courses by Month
Please choose a link below to view upcoming courses by a particular month.
Indicates courses for Dietary Supplement companies
January 2012
February 2012
Feb. 7,
SOP and Record Keeping for Compliance to 21 CFR 111, California
Feb. 8, Process Definition & Control; Facility / Utilities Design & Monitoring,
California
Feb. 14-15, 21 CFR 111 Dietary Supplement GMP Overview, California
Feb. 21,
Corrective Action and Management, Florida
Feb. 22,
FDA Inspection Readiness, Florida
March 2012
Mar. 7-8,
FDA Inspection Readiness and
SOP and Record Keeping for Compliance to 21 CFR 111 prior to Expo West, California
- Mar. 13-15, Registering Drug Products in the EU: Quality (CMC) Requirements,
Boston, MA
Mar. 20, SOP and Record Keeping for Compliance to 21 CFR 111,
Salt Lake City, UT
Mar. 21, Process Definition & Control; Facility/Utilities Design & Monitoring,
Salt Lake City, UT
Mar. 27-28, 21 CFR 111 Dietary Supplement GMP Overview, Salt Lake City, UT
- Mar. 27-29,
Formulation & Processing Part 2 (QLP3b), Boston, MA
April 2012
- Apr. 2, Statistical Process Control for Pharmacutical Manufacturing, San Mateo, CA
- Apr. 3-4,
The Role of the European Qualified Person (QP), Boston, MA
Apr 10-12,
Testing Method Selection, Specification Setting & Equipment,
New Jersey
Apr. 17,
Corrective Action and Management, Salt Lake City, UT
Apr. 18,
FDA Inspection Readiness, Salt Lake City, UT
Apr. 19,
Stability Program Development, Salt Lake City, UT
- Apr. 24,
Workshop – Extractables and Leachables Requirements in Pharmacutical Development, Boston, MA
April 24,
Cleaning and Control of Cross-Contamination, California
Apr. 25-26,
Risk Assessment and Risk Management, California
May 2012
May 8-9,
Vendor Qualification & Audit Training (other courses TBD), prior to Supply Side MarketPlace, New York
May 15,
Cleaning and Control of Cross-Contamination, Salt Lake City, UT
May 16-17,
Risk Assessment and Risk Management, Salt Lake City, UT
- May 24,
Workshop – Best Practices for Deviation and CAPA Management(1/2 day spent on each topic), Boston MA
May 30,
FDA Inspection Readiness, California
May 31,
Corrective Action and Management, California
June 2012
Jun. 5-6,
Vendor Qualification & Audit Training, Salt Lake City, UT
- Jun. 12-14,
Pharmacutical Microbiology (QLP4), Boston MA
Jun. 12-14,
Testing Method Selection, Specification Setting & Equipment, California
Jun. 13,
Cleaning and Control of Cross-Contamination, New Jersey
Jun. 14,
Process Definition & Control; Facility/Utilities Design & Monitoring, New Jersey
Jun. 14-15,
Risk Assessment and Risk Management, New Jersey
- Jun. 15,
Workshop – Laboratory GMP Requirements (1/2 day on requirements, 1/2 day on Investigating Out of Specification Results), Boston MA
- Jun. 25-29,
Effective Pharmaceutical Audits and Self-Inspections, Boston MA
July 2012
August 2012
September 2012
October 2012
November 2012
Nov. 5-6,
Vendor Qualification & Audit Training, (Other courses TBD) prior to Supply Side West, Las Vegas, NV
Nov. 13-14,
Staff Recruitment and Internal Training Development, New Jersey
- Nov 13-14,
Effective Quality Systems for Research and Deveopment, Boston MA
Nov. 13-14,
International Regulatory Requirements for Dietary Supplements,
Salt Lake City, UT
December 2012