About Pharmatrain

PHARMATRAIN has developed a host of unique and customized job-oriented courses that help you gain expertise, enhance your credibility as a technical professional and provide the relevant practical and theoretical knowledge of the pharma domain. The fact that the training modules are designed and delivered by experienced pharma professionals means that you develop competence that is readily deployable.

Core team

GNV Chandra Sekhar Reddy, M.Sc

A qualified and qualitative Pharmaceutical Professional extensively worked for organizations of repute in India and also an expert trainer who was instrumental in running Pharmatrain successfully for the last 10 years providing necessary skillful knowledge to improve the employability of students.

A Maheshwara Reddy, M.Pharm., PMP

A proven industry veteran in the organizations of repute in India with a commendable track record of providing overall clinical research and development in analytical chemistry, method development, validation, and complex technical investigation, ensuring (cGMP) Good Manufacturing Practices have adhered. A quick problem solver with resolution skills, analytical expertise, and extensive knowledge of FDA requirements for ANDA submissions. He is also a certified Project Management Professional (PMP).

Advisory Team

M S Sarveswara Rao, M.Pharm

Expert Pharmaceutical formulation technology professional with Comprehensive Rx & OTC GENERIC background in Product Development and processes from Concept to Launch. A proactive, energetic, and highly motivated senior pharmaceutical technology professional with exceptional hands-on formulation experienced in research & development and project management. He also spearheaded Packaging function entirely during his long stint in the Pharmaceutical Industry with organizations of repute in India.

K Tata Rao, M.Pharm., FIC

He is well-known entrepreneur in the past 40 years and instrumental in bringing several first to launch finished dosage forms in India. His academic prowess led many a successful entrepreneur inducted into the pharmaceutical industry. Most of his team members have been instrumental either in running successful organizations as key professionals or starting his / her own ventures. He is an active member of IPA, AP State Branch as Principal Office Bearer, also closely associated with Organization of Pharmaceutical Manufacturers (OPM), and National Alliance of Pharmaceutical Manufacturers’ Association (NAPA). He is also one of the founder trustees of IPA AP Trust.

Expert Team

K Subbi Reddy, M.Pharm., LL.B

Subbi Reddy Karri has retired as Joint Director, A.P.Drugs Control Administration in 2013 after serving the Dept for a period of 30 Years in different capacities. He worked in Pharmexcil on deputation for four years and handled many regulatory issues including bar coding. He is also well versed with Procurement of Medicines as he has worked with A.P. Health, Medical Housing and Infrastructure Development Corporation (APHMHIDC) as General Manager. He is one of the members from India to draft and sign Trade Agreement between India and Russia.

He is the recipient of the A.P.CM appreciation letter as the best Drugs Inspector during the year 1989. He is a resource person and trainer for many pharma companies and training Institutes on regulatory and personality development topics. He is the practitioner of Sahaja Yoga founded by H.H.Shri Mataji Nirmala Devi since 1991.

Dr Subramanian Iyer, M.Pharm., Ph.D

Dr. Subramanian Iyer has around twenty-three years of pharmaceutical experience with focus on Quality Management Systems and Analytical Chemistry. He worked at organizations of repute such as Orchid, Ranbaxy, IPCA and Waters India, handling Analytical Development and Formulations R&D. Currently working with Mylan Laboratories Ltd as Head of OSD Quality-India FR&D (Finished Dosage Forms). He was instrumental in facing several global regulatory audits successfully. He has several publications in renowned journals. He continues to guide pharmacy students for their research / thesis work. He is presently a member of USP South Asia Stakeholder Forum, invitee for several workshops arranged by USP to understand industry perspective.

Dr Raman Nanduri, M.Sc., Ph.D

A well-known Pharmaceutical Professional having 28 years of proven experience in the field of API Manufacturing deploying Analytical Applications, Quality Systems, and Quality Culture in the organizations of repute. He has several publications in renowned journals. He also participated several pharma workshops globally. Currently he is Director, Analysis Lab Pvt Ltd. He gave a number of speeches inspiring many students at various colleges in Telangana and AP on Analytical Development, Quality Systems and Culture.

V Sivarami Reddy, M.Pharm

Results-driven and dedicated Pharmaceutical Manufacturing Professional with wide-ranging experience in planning and leading operations involving small- to medium-sized manufacturing environments in the organizations of repute in India. He was instrumental in evaluating, designing, and implementing continuous process improvements to minimize waste and reduce costs while maximizing quality and yield. Established effective quality control and safety programs, encouraging proactive participation across the manufacturing floor. Excellent communicator; success building cohesive teams focused on production goals, safety, and throughput. He spearheaded Projects function as well effectively and efficiently during his stint in the industry.

We also have affiliations with eminent people who proved their worth with academic as well as technical capabilities in varied streams across the Indian Pharmaceutical Industry and would be available for valuable guidance for the team.


Pharmatrain should be the most sought-after training institute in the next five years for all the Science, Pharma, Chemical and Biotechnology Graduates and Post Graduates for their career solutions (from novice to the professional).


Identify the gaps in the knowledge, skillsets and effectively bridge by imparting training interventions there to produce qualitative professionals who can effectively deal with any regulatory inspections with ease and compliance.