USFDA

ISPE

MHRA

WHO

PIC/S

QC

USFDA

ISPE

MHRA

WHO

PIC/S

QC

USFDA

ISPE

MHRA

WHO

PIC/S

QC

USFDA

ISPE

MHRA

WHO

PIC/S

QC

USFDA

ISPE

MHRA

WHO

PIC/S

QC

USFDA

ISPE

MHRA

WHO

PIC/S

QC

  • Going the extra mile

Beyond Project Management

For any consultancy company in the field of Pharmaceutical Engineering, a defined set of deliverables define their business model. For Pharma Access, we strive to add value at every step of the project leaving no stone unturned towards successful completion of the Turnkey Pharmaceutical Engineering. Hence, we are not merely a Project Management firm, but we go beyond project management and support our client in decision making at every step.

Let us see how we go beyond client’s expectation to achieve desired results:

One of the major activities during initial phases of the Project cycle is performing FAT i.e. factory acceptance test for the machines and equipment and check that they perform as per the accepted User requirement specifications etc. Pharma Access not only co-ordinates for successful FAT but also is involve in finalizing parameters to be tested and are crucial for any machine to perform. The various stages of this activity are:

  • Preparation of change part drawings
  • Approvals on DQ
  • Procurement of testing material like filling bottles, packaging material like PVC films etc. of desired dimensions for finished product
  • Performing Pre-FAT by Pharma Access personnel
  • Scheduling of FAT as per export schedule and project execution schedule
  • Performing FAT and checking desired parameters
  • Recommendation and Modification as per FAT observation
  • Performing re-FAT post compliance of earlier FAT findings
  • Spare parts and change parts requirement assessment
  • Packaging recommendation as per export norms

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