Qualification and Validation

User Requirements Specifications (URS).

GMP design review.

VMP Validation master plan.

System impact assessment.

Design Qualification DQ.

Risk management and risk assessment.

Qualification protocol and implementation ( IQ, OQ, PQ).

Computerized system Validation

Cleaning Validation/Process Validation/Method Validation Training.

GMP Compliance

GMP gap analysis.
QMS quality system upgrade.
Data integrity DI management system.
GMP training.
Third party audit.
Accompanied by GMP certification inspection and audit.
Mock audit.
R&D/Technology Transfer Consulting.
GMP project management consulting.
Automation/information technology/

intelligent planning.

Contact us

Phone/fax:

0756-2666960.
Mobile phone: 13392961199

(Manager Sun).

E-mail:BD@bioandpharm.com

Address:

604, Block A, Yuexing Industrial Building, No. 108 Xinghua Road, Xiangzhou District, Zhuhai City.