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Design of Experiments and Statistical Process Control for Process Development and Validation 2017

Design of Experiments and Statistical Process Control for Process Development and Validation 2017

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Who should attend?

Directors Managers Supervisors Lead workers in Process Development Manufacturing Regulatory Affairs Quality Assurance and Quality Control Workers who will be participating in operations or the supervision of the development, manufacturing, or testing of medicinal products will benefit from knowing the procedures and applications of DOE and SPC.

Details

 

Course "Design of Experiments and Statistical Process Control for Process Development and Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

               

Overview:

 

This course will present the procedures that must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes. A practical approach with case studies and examples will be used, with theoretical information introduced only when necessary to understand an experiment. Examples from real processes and testing procedures will be used to present the student with examples that will be directly applicable to their work.

 

Why you should attend:

 

Any pharmaceutical worker who performs, supervises or reviews manufacturing or testing processes needs to understand the relationships among the process parameters and be able to monitor the performance of processes and test methods. This is particularly true for the worker in Quality Control and Quality Assurance as the recent FDA guidance document on Process Validation has assigned the responsibility for reviewing and interpreting DOE and SPC studies to the Quality Unit. The work, however, is done by the development, manufacturing, or quality systems worker who should also attend this course to learn how to design the systems and studies, and interpret the results generated.

 

Who will benefit:

 

  • Directors
  • Managers
  • Supervisors
  • Lead workers in Process Development
  • Manufacturing
  • Regulatory Affairs
  • Quality Assurance and Quality Control
  • Workers who will be participating in operations or the supervision of the development, manufacturing, or testing of medicinal products will benefit from knowing the procedures and applications of DOE and SPC.

 

 

 

 Location: Kuala Lumpur, Malaysia Date:  November 16th & 17th, 2017 and Time: 9:00 AM to 6:00 PM

Venue: WILL BE ANNOUNCED SOON , Kuala Lumpur, Malaysia

 

Price:

 

Price: $895.00 (Seminar Fee for One Delegate)

Register for 5 attendees   Price: $2,685.00   $4,475.00 You Save: $1,790.00 (40%)*

Register now and save $200. (Early Bird)

Until October 10, Early Bird Price: $895.00 From October 11 to November 14, Regular Price: $1,095.00

Register for 10 attendees   Price: $4,922.00  $8,950.00 You Save: $4,028.00 (45%)*

 

 

Contact us today!

 

NetZealous LLC DBA GlobalCompliancePanel

john.robinson@globalcompliancepanel.com  

support@globalcompliancepanel.com 

Toll free: +1-800-447-9407

Phone: +1-510-584-9661

 Website: http://www.globalcompliancepanel.com

 

Registration Link - http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901327SEMINAR?pharmiweb-November-2017-SEO

Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/

Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/

Follow us on Twitter: https://twitter.com/GCPanel

 

 

Prices

Price: $895.00 (Seminar Fee for One Delegate) Register for 5 attendees Price: $2,685.00 $4,475.00 You Save: $1,790.00 (40%)* Register for 10 attendees Price: $4,922.00 $8,950.00 You Save: $4,028.00 (45%)* Register now and save $200. (Early Bird

Contact

Event Manager
john.robinson@globalcompliancepanel.com

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