cGxP

Consulting

 

 

VALIDATION

 

DRUG SOLUBILITY

DRUG UNIFORMITY

 

 MICROBIOLOGICAL

 

SOPíS SPECIFICATIONS, TEST PROCEDURES

PRESERVATIVE SYSTEM

WATER SYSTEM

 

  ACTIVITY

 

F.P. PARTICLE SIZE SPECIFICATIONS

VISCOSITY

 

 MANUFACTURING FACILITIES AND EQUIPMENT

 

CHEMICAL/MICROBIOLOGICAL ISSUES

 

 CLEANING VALIDATION

 

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