About Us

T.Rama Rao
T.Rama Rao – Sr. Consultant & Promoter

Basic Qualification: M.Pharm in Pharmaceutical Technology, Year 1985, Andhra University, Visakhapatnam.
Work Experience: More than 30 years of experience

Mr.T.Rama Rao is an Industrial Pharmacist with more than of 30 years of experience. He was awarded G.P.Nair Gold Medal by Indian Drug Manufacturers Association (IDMA), Mumbai & Nageswara Rao Pantulu Gold Medal by Andhra University for standing first In B.Pharm, 1983.and awarded Project Excellency award by Procter & Gamble Hygiene and Health Care Ltd, Baddi. Mr.Rama Rao has established the Sai Pharma Consultancy about two years ago with a vision to provide the services, Design & Engineering, Auditing and Compliance Management, DMF Compilation and Submission Support, Formulation Development & Technology Transfer & GxP Training etc to Pharmaceutical, Medical Devices, Biotech and AYUSH Industry to mainaintain in perpetually compliant state. He has a wide range of experience in the mentioned services and discharged at executive as well as leadership responsibilities. He is an active member of professional Associations like Indian Pharmaceutical Association (IPA) .He is a technical Consultant for Andhra Pradesh MedTech Zone Ltd (AMTZ), Visakhapatnam. He is a former Consultant (Drug & Laboratory) PMU for Central Drug Standards Control Organisation (CDSCO) New Delhi under Ministry of Health and Family Welfare (MoHFW) GOI, New Delhi. He is a regular speaker in industry & academia seminars.

A.G. Ganu
Mr.A.G. Ganu, Director Projects

Basic Qualification: BE in Electrical – in 1971 from B. I. T. S. (Birla Institute of Technology) Pilani. Diploma in Digital Electronics - 1983 from VRCE, Nagpur & Diploma in Business Management & Administration - 1983 from Nagpur University.
Work Experience: An engineer with more than 35 years of experience

An Engineer with more than 35 years of experience in Facility Design & Project Management.
Mr.A.G.Ganu rendered his services to provide Design & Engineering services to industry sectors like Formulations, Bulk Drugs, Biological Products (Vaccines) & IV Fluids. It covers HVAC, Electrical, Water Systems, Equipments, Steam and Piping & Insulation. . He has a wide ranging experience in all aspects of project management right from concept planning to start up. He has worked with and handled many projects.
Some of the major projects handled include at Biologial E Limited, Hyderabad ( A P ):
a) Set up a State of the Art green field project at Shameerpet in a span of two years, for Human Vaccines with an investment of approximately USD 50million,
b) State of the Art green field project for Liquid Orals Facility at Deheradun, with an investment of approximately USD 10 million
c)Up-graded the existing Antigen facility ( TT ), up – graded existing Breeding Facility & built up a new additional Animal Breeding Facility at Gagan Pahad with a project cost of USD 10 million.
Ranbaxy Laboratories Limited, Dewas ( M P ) : d) Set up a facility for Cephalosporin’s – Liquid & Powder Injectables, Tablets & Capsules project cost was approximately USD 20 million,
Maharashtra Antibiotics & Pharmaceuticals Ltd, Nagpur ( Maharashtra ): e) Set up a facility for formulations of Tablets, Capsules & Liquid & Powder Injectables.
f) Various other projects like Bharat Parenterals, Baroda, PDPL, Indore, Phimex Bulk Drugs, Hyderabad, Alkyl Amines, Vazir Glass etc.
He is an active Member of various bodies like Indian Institute Of Plant Engineers, ISHRAE – India,
Indian Association of Vaccinology and Former member of ISPE (International Society of Pharmaceutical Engineers), International Institute of Validation.

Dr. S. RAVIPRAKASH REDDY M.Sc, MBA, Ph.D. , - Director ,Regulatory Affairs

Basic Qualification: Master’s Degree in Clinical Research and Regulatory Affairs, Masters in Business Administration and Post doctorate in pharmaceutical sciences.
Work Experience: More than 25 years of experience

Dr.Ravi has over 25 years of combined experience in dealing with several Active Pharmaceutical Ingredients (APIs), finished dosage forms, Medical Devices, Nuetraceuticals and clinical research.
He has experience in compilation and review of Drug Master Files, Active Substances Master files, Certificates of Suitability (CEP), ICH eCTD requirements for CMC, ANDA for US Submissions, ANDS for Canadian Submissions, adequate exposure in compilation of dossier in EU eCTD for EU and Australian requirements, ASEAN CTD requirements for ASEAN registrations.
He has also experience in monitoring clinical studies and reviewing protocols, reports and study monitoring. He has experience in interfacing with various global regulatory agencies and handled many audits from USFDA, TGA, Health Canada, CDSCO, MHRA, EDQM and other EU agencies.
He is also extensively travelled globally for business needs and attended many global trainings and seminars in his fields of expert. He worked with companies like Dr.Reddy’s Laboratories, Perrigo Company USA, Granules India Limited, Life Pharma, Vivimed Labs Limited and various CROs in formulations development and Clinical research.

V. R. MAJUMDAR - Director Operations (API & Chemicals)

Basic Qualification: B.Sc (Tech) specialized in Technology of Pharmaceuticals and Fine chemicals from University Institute of Chemical technology (UICT) Mumbai in 1984.Formerly known as UDCT.
Work Experience: More than over 33 years of experience

Mr.Majumdar is having overall experience of 33 years in Pharmaceutical Industry in field of
► Designing of API facilities with Basic Engineering, Detailed Engineering, Conceptual designs as per the current cGMP norms with including Project implementation and co-ordination,
► Designing and Executing Common effluent treatment plants with state of art technology confirming to Zero Liquid Discharge Norms laid down by Pollution Control Board
► Process Management, Quality / EHS Compliance, New Product Development Implementation in Bulk Drug and Chemical Industries
► Proven abilities in effectuating cost saving and energy saving techniques/ measures and modification to achieve substantial reduction in operational work within the budget.

Dr. Kumar V.S. Nemmani
Dr. Kumar V.S. Nemmani M. Pharm., Ph.D. , Director - Pharmaceutical Development

Basic Qualification: Postdoctoral Fellow, McGill University, Montreal, Canada in Feb. 2005 Doctor of Philosophy, NIPER, Chandigarh , Feb. 2002 , Master of Pharmacy (Pharmacology), AU, Visakhapatnam Jul.1995
Work Experience: More than 13 years of experience

Dr.Kumar has more than 13 years of rich experience Pharmaceutical Development in drug discovery and development. Expert at In vivo screening for various indications. He has established and led biological research labs for various disorders. He is capable in managing the Overall product lifecycle management. He has presented scientific work in national and international conferences and has total 39 publications (Pub Med) in international journals. He has presented 20 oral and poster presentations at national and international conferences. He has worked in leadership roles at Dr. Reddys Research Foundation, Piramal Enterprises Ltd & Lupin Ltd. Presently he is heading the academic, administrative and research activities at Shri Vishnu College Pharmacy, Bhimavaram.

Ms. T.Manjula
Ms. T.Manjula – Director Finance

Basic Qualification: Graduate from Andhra University, Visakhapatnam in the year 1985
Work Experience: More than 30 years of experience.

Ms.T.Manjula is well versed with finance management with more than 30 years of experience. in family owned financial management. She oversees, review, and adhere to the budgets for each business department. Analyse the financial climate and market trends to assist senior executives in creating strategic plans for the future. She combines operational and strategic roles, manage accounting and financial control functions, and establish a financial strategy for the profitable long-term growth.

Why Us

A few reasons to partner with us

You get all services with regards to GMP requirements for US FDA, UK MHRA, TGA, PIC/S, WHO GMP, etc., Project Management, Pharmaceutical Development, Audits & Compliance Management, Regulatory Affairs, GxP Training all at Sai Pharma Consultants.

Commitment to Our Clients

We endeavor to deliver on our commitments to our clients, focusing on transparency, results and high standards. We provide tailor-made solutions to meet clients, business and project goals. We aim to build long-term relationships with our clients that are founded on trust.

Commitment to Quality & Delivery

We are committed to quality work and on time delivery through the development and implementation of our Quality Management System. We aim to deliver the highest level of professional excellence.

Experience in Industry

With over more than 30 years of experience in industry and covers our services to a wide variety of Pharmaceutical & Biotech ,Ayurvedic, Homeopathic, Excipients and Packaging material industries..

Commitment to Economic & Sustainable Design

We emphasize on economical ,designs with high production & energy efficiency specific needs and situations to improve the customer experience and business performance against rising competition and Reducing Costs..