BioPractice
Princeton, New Jersey, United States of America
BioPractice as a platform focuses to be the core part of learning and development for the life science industry as well as the academia. It has been built to meet the objective of the learning and development in the areas of latest trends and practices of the industry, regulation updates in the industry, research and development for the discoveries and development as well as to reflect the industry real time practices for the academia.
The platform also focuses to support the industry on the USFDA,EMA and APAC Regulations and practices for the core development of any business organisation. These learning and development are been implemented or supported through various streams like webinar, seminar and onsite trainings.
They collaborate with world class consultants to bring in their hands on experience of working with regulatory bodies and also to assist companies on updating or executing the latest trends or practices on the regulations, insights into the areas of research and development for the companies as well as to assist in launching a new product or service into the same or new country.
The platform also focuses to support the industry on the USFDA,EMA and APAC Regulations and practices for the core development of any business organisation. These learning and development are been implemented or supported through various streams like webinar, seminar and onsite trainings.
They collaborate with world class consultants to bring in their hands on experience of working with regulatory bodies and also to assist companies on updating or executing the latest trends or practices on the regulations, insights into the areas of research and development for the companies as well as to assist in launching a new product or service into the same or new country.
CONFERENCES AND COURSES
International Seminar on Corrective And Preventive Action In FDA Regulated Industry
Webcast
Quality Management
May 12, 2017
Biosimilar Orphan Drugs : The Next Regulatory Challenge 2016
- Webcast
- Biotechnology, Healthcare Management
- Oct 21, 2016
NO More Written Procedure (Standard Operating Procedure - SOP) Related Observations, Citations or as an Annual Top Ten FDA Observation Finding Completely Achievable With the Provided Knowledge, Skills, Techniques and Methods
- Webcast
- Healthcare Management
- Oct 14, 2016
How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare
- Webcast
- Quality Management
- Jun 30, 2016
Supplier Management in FDA - Regulated Industry
In-Person Event- Biochemistry and Molecular Genetics, Asthma Clinical Immunology ...
- Oct 22, 2015
Princeton, New Jersey, USA
FDA Inspections, Warning Letters, and CAPA 2015
- In-Person Event
- Biotechnology, Cell and Developmental Biology ...
- Sep 30, 2015
- Princeton, New Jersey, USA
9th International seminar on Biosimilars
- In-Person Event
- Biotechnology, Cell and Developmental Biology ...
- Aug 14, 2015
- Princeton, New Jersey, USA
9th International Seminar the Importance of All Senior Management Roles in FDA Compliance
- In-Person Event
- Biotechnology, Practice Management ...
- Jul 10, 2015
- Princeton, New Jersey, USA
7th International Seminar Corrective And Preventive Action In FDA Regulated Industry
- In-Person Event
- Biochemistry and Molecular Genetics, Biotechnology ...
- Apr 30, 2015
- Princeton, New Jersey, USA
Quick Links
- 50 Division Street, Suite 501,
- Somerville, NJ 08876
- support@emedevents.com