Tuesday, June 22, 2010

Pharmaceutical Events -28-29-June 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry

Event Details: Preparing And Facing Regulatory Audits: A Practical Approach
Speaker: Maija Hietava-Lorenzi
Date & Venue:17-18 June 2010, Istanbul, Turkey

Details: The QC laboratory is essentially responsible for more than 50% of product safety and efficacy if you consider that they test raw materials, in-process materials and finished product, as well as perform stability testing, tests for process validation, cleaning validation, equipment validation and other validations and they also develop and validate analytical methods. Any company therefore relies heavily on the integrity of the data provided by its QC laboratory. This course will provide a detailed review of current regulatory requirements relating to GMPs in the laboratory as well as current industry practices.

The Workshop Leader for this event is Maija Hietava-Lorenzi, who has tremendous experience and expertise in this area. Maija used to be registered in EMEA as an EMEA Expert. She has represented the EU Commission, PQ program of WHO Geneva, and National Agency for Medicines Finland, as a Senior Pharmaceutical Inspector. She has worked in WHO PQ programme and performed GMP and GCP inspections worldwide. She has a wide experience in different positions in pharma industry and latest in biotech industry as VP - QA and Analytical Development, FIT Biotech and QP in Ark Therapeutics Oy in Finland.

for more info visit:www.pharmasupport.in

Get registration for this event visit: pharma-event-registration

Pharmaceutical Events -21-25-June 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry.

Event Details: Preparing and facing Regulatory Audits: A Practical Approach
Speaker: Maija Hietava-Lorenzi
Date & Venue:21-22 June 2010, Mumbai, 24-25 June 2010, Hyderabad

Details: The Workshop Leader for this event is Maija Hietava-Lorenzi, who has tremendous experience and expertise in this area. Maija used to be registered in EMEA as an EMEA Expert, when working in the Finnish Medicines Agency as a Senior Inspector. She has represented the EU Commission, PQ program of WHO Geneva, and National Agency for Medicines Finland, as a Senior Pharmaceutical Inspector. She has also been an Instructor in the Regulatory Compliance School, Ministry of Health in Italy, and has conducted various inspections on behalf of the EU Commission EMEA, NAM, PIC/S, and also AFSSAPS France with French Inspectors through an exchange program of European Commission. She has worked in WHO PQ programme and performed GMP and GCP inspections worldwide. In Africa she has worked in different programs for WHO, WHO PQ and AEDES. She has a wide experience in different positions in pharma industry and latest in biotech industry as VP - QA and Analytical Development, FIT Biotech and QP in Ark Therapeutics Oy in Finland.

for more info visit: www.pharmasupport.in
Get registration for this event visit: pharma-event-registration

Pharmaceutical Events -17-18-June 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry.

Event Details: Preparing And Facing Regulatory Audits: A Practical Approach
Speaker: Maija Hietava-Lorenzi
Date & Venue:17-18 June 2010, Istanbul, Turkey

Details: Pharma companies have always concentrated on building systems for quality - conscious drug manufacturing. At a foreign regulatory audit, however, it is not only the company image that is projected; it is also the professional culture as well as knowledge base that leave a lasting impact. In spite of facing many regulatory inspections, Pharma companies still lack finesse, detailed preparedness and a systematic approach while facing most regulatory inspections.

For this program, our industry expert, Maija Heitava – Lorenzi will share her experience and expertise as a Regulator and Inspector, as well as provide valuable inputs on the Do’s and Don’ts of an audit. Whether it is a self-audit or whether it is the EU, USFDA or MHRA, this course provides practical points on getting it right the first time, every time.

for more info visit:www.pharmasupport.in

Get registration for this event visit: pharma-event-registration