PHARMACEUTICALS 2011 - Validation of Bioanalytical Assays for Biologicals

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Category Bioanalytical Assays Validation; Bioanalytical Assays for Biologicals; validation protocol; assay validation method; regulatory guidelines; assay development

Deadline: November 30, 2011 | Date: November 30, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2011-11-14 20:07:53 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

Strategic management of the pharmacokinetic profile of a drug is a critical determinant of therapeutic success in the clinic. Successful development and validation of the bioanalytical assays that support these studies are key components to the process.

Areas Covered in the Seminar:

- Expectations of the GLP (GCLP) environment.

- Effective assay development.

- Maximizing precision and accuracy.

- Minimizing matrix effects.

- Setting specifications for the validation protocol.

- Sample re-analysis plan.

- Managing the life cycle of the bioanalytical assay.

NOTE : Use this Promocode (128600) to avail 10% discount, valid upto 28th November 2011.