About Us

Amogha Pharma Consultancy was started by Dr. Gurudatta GG in Feb 2006 ,having a vast experience of 22 years in various areas of Pharma Industry.

He has worked in Quality Control department, Quality assurance department, Analytical Development, Regulatory Affairs and formulation Development. He has been trained by WHO Geneva for Quality Management systems.

He has faced and successfully cleared many international regulatory audits like MCC South Africa, MHRA UK, TGA Australia, WHO Geneva, and USFDA. Apart from this he has faced many international clients audits also.

He was working with Strides Arcolab Limited, Bangalore and IPCA Laboratories (Athal Plant) as Head QA.

Presently Amogha Pharma consultancy has many clients in soft gelatin capsules manufacturing, Tablets and liquid orals manufacturing plants, sterile products manufacturing unit ( SVP) and API manufacturing facility.

There are many technical experts who are supporting externally to Amogha Pharma consultancy who have got more than 30 years experience.

Amogha Pharma Consultancy was started with an aim of providing Total Pharma Business solutions to organizations.

We give consultancy in various areas of Pharmaceutical business as mentioned below:

  • Quality Management system design and implementation; monitoring of quality system and quality of the products manufactured at plant level.
  • Analytical method development and method validation
  • Formulation development for Para 3 filings ( Generic formulations)
  • Formulation development for Para 3 filings ( Generic formulations)
  • Training : GMP, GLP, GCP and evaluation of training
  • Auditing: Third party auditing of API, Pharmaceutical formulations plants, Clinical research Organisations facilities.
  • Project Management: From Conceptualization, design and construction to Qualification and validation of Equipment and systems
  • Contract Manufacturing of Pharmaceutical formulations
  • Dossier management: Dossier preparation and submission
  • Contract manufacturing of Cosmetics for various countries
  • Clinical research: Phase -2 , Phase 3 and Phase 4 trials and Bioequivalence studies
  • Placement services