Advisory Team

Merugu Raju

Principal Consultant

Dr. Merugu Raju, M.Pharma, Ph.D.

Principal Consultant - Formulation Development & Technology Transfer

Dr. Merugu Raju brings over 25 years of experience in the pharmaceutical industry, specializing in the design and development of oral drug delivery systems, including NDDS (Novel Drug Delivery Systems), to meet the demands of developed markets.

Key Experience:

• Worked with leading pharmaceutical companies like Medley Pharmaceuticals Ltd, MSN Laboratories Ltd, Medreich Laboratories Ltd, Ipca Laboratories Ltd, and Macleods Pharmaceuticals Ltd.
• Expertise in formulation development and technology transfer, contributing to the successful launch of various pharmaceutical products in regulated markets.

Dr. Raju’s depth of experience in formulation and drug delivery systems has made him a trusted consultant in the pharmaceutical industry.

Rajendraprabhu

Sr. Consultant – Biotechnology Projects

Dr. Rajendraprabhu, Ph.D.

Sr. Consultant – Biotechnology Projects

Dr. Rajendraprabhu is an expert in immunobiologicals with over 35 years of experience. He has been instrumental in the development of various anti-serums and vaccines, including:

• Anti-gas gangrene serum
• Anti-snake venom serum (ASVS) for both Indian and African snake venoms
• Diphtheria, Pertussis, and Tetanus vaccines (DPT)
• ARS, ADS, ATS, and scorpion venom anti-serum

Dr. Rajendraprabhu has worked at renowned institutions like King Institute of Preventive Medicine, Mediclone Research Centre, and Blue Whale Biological Ltd. He also led the development of an anti-cancer drug derived from snake venom components and has expertise in antigen purification, RIA, and ELISA.

His extensive experience in immunobiologicals and biotechnological innovations positions him as a leader in his field.

Sudesh Kumar

Sr. Consultant – HVAC & Clean Room Solutions

Sudesh Kumar H N

Sr. Consultant – HVAC & Clean Room Solutions

Mr. Sudesh Kumar H N is an experienced professional with 30 years of expertise in HVAC and clean room solutions. He has successfully completed numerous projects, particularly in the pharmaceutical and healthcare sectors, ensuring compliance with stringent industry standards for clean environments.

Key Projects & Clients:

• Indian Institute of Science (BSL-2 projects)
• Strand Life Sciences Pvt. Ltd.
• Jubilent Biosys (Two Projects)
• RANBAXY Nigeria Africa
• Nigerian German Chemicals (NGC)
• Strides Arcolab Ltd.
• Reich India
• SEQUENT LAB
• AFDIL (Anglo French Drug Industries)
• Karnataka Antibiotics and Pharmaceuticals Ltd.
• SOLECTRON CENTUM
• Meyer Organic Pvt. Ltd.
• Kanachur Hospital
• HCG Curie Centre of Oncology
• BGS Apollo Hospital

Sudesh Kumar has an impressive portfolio of high-profile projects across diverse industries, demonstrating his ability to design and implement efficient HVAC and cleanroom systems for pharmaceutical manufacturing, biotech facilities, hospitals, and research labs.

Sanjay Shukre

Sr. Consultant – Projects Management

Sanjay Shukre

Sr. Consultant – Projects Management B.E. (Electrical), FIETE, MIE, C.Engg.

Mr. Sanjay Shukre has 30 years of experience in the pharmaceutical industry, specializing in electrical, HVAC, utilities, and project management. He has successfully led the setup of formulation facilities and pharma utilities, ensuring compliance with USFDA, MHRA, TGA, and WHO guidelines.

Key Expertise:

• Project Setup & Execution: Design and execution of pharmaceutical facilities and utilities.
• Pharma Utilities: Boilers, chillers, HVAC, water systems, and generators.
• Compliance & Design: Electrical panel design, ETPs, and regulatory adherence.

Notable Projects:

• EDS Pharma, Congo
• JCS Humanity, Georgia
• Ushma Technologies, Pithampur
• Paras Pharmaceuticals, Baddi

Shukre is skilled in project planning, vendor management, and ensuring on-time project delivery while maintaining regulatory standards.

Samir Vasavada

Sr. Consultant – Pharma Operations

Samir A. Vasavada

Sr. Consultant – Pharma Operations M.Pharma

With 35 years of experience in the pharmaceutical industry, Mr. Samir Vasavada has worked across diverse domains such as pharma production, supply chain, techno-commercial operations, clinical research, tech transfer, and packaging development. He has held key positions at Abbott India Ltd., Knoll Pharmaceuticals Ltd., Boots Pharmaceuticals Ltd., and Pfizer Ltd.

Key Expertise:

• Pharma Production & Supply Chain
• Tech Transfer & Clinical Research
• Packaging & Label Management
• External Manufacturing

Vasavada has a wealth of experience in strategic manufacturing and external collaborations, driving operational excellence and efficiency in global pharmaceutical operations.

Sunil Kanvinde

Sr. Consultant – Life Science Management

Dr. Sunil Avdhut Kanvinde

Sr. Consultant – Life Science Management M. Pharm, Ph.D. (Tech), D.I.M., LL.B.

With 35 years of experience in the pharmaceutical industry, Dr. Sunil Kanvinde has held leadership roles across multiple pharmaceutical companies. He has expertise in production management, contract manufacturing, tech transfer, quality compliance, and global supply chain management.

Key Expertise:

• Pharma Manufacturing & Production
• Tech Transfer & Outsourcing
• Packaging Development
• Regulatory Compliance & Audits
• Project Management for Regulated Markets

Dr. Kanvinde has worked with German Remedies, E. Merck India, Novartis India, Sandoz, Ranbaxy, Apotex, Pfizer, and Sri Krishna Pharmaceuticals, managing large-scale operations and driving pharmaceutical development across regulated markets.

Yuvaraj

Principal Consultant – Clinical Research

Dr. Yuvaraj (Pharm)., Ph.D., D.Sc

Principal Consultant – Clinical Research

Dr. Yuvaraj has extensive qualifications and over 20 years of experience in clinical research, preclinical studies, and drug discovery. He holds advanced degrees in medicinal chemistry and has focused his research on cancer mechanisms and newer pharmacological molecules.

Key Expertise:

• Clinical Trials & Auditing (Phase I to III)
• Preclinical & Bioequivalence Studies
• Regulatory Compliance & Audits
• Quality Systems Auditor (ISO 17025, ISO 9001, ISO 15189, ISO 27001)
• Therapeutic Areas: Oncology, Endocrinology, Respiratory, CNS
• Regulatory Authority Inspections (USFDA, EMA, WHO, ANVISA, DCG(I), MedSafe)

Dr. Yuvaraj has conducted audits globally (India, Africa, Canada, Europe) and has been instrumental in auditing clinical studies and systems development. He is a Chartered Scientist (C.Sci.) and has received numerous awards and recognition for his contributions to the field.

Murugesan

Sr. Consultant Projects & Engineering

N. Murugesan

Sr. Consultant Projects & Engineering

With over 30 years of experience in the pharmaceutical and engineering sectors, N. Murugesan has successfully led multiple greenfield projects and engineering initiatives in pharma manufacturing.

Key Expertise:

• Project Management (Greenfield Projects, Plant Setups)
• Engineering & Maintenance (OSD, Topical Solutions, Vaccine Manufacturing)
• HVAC & Modular Clean Room Projects
• Sterile Injectable Plant Commissioning & Validation
• Cross-Functional Leadership (Project Planning, Procurement, Execution)

Key Roles:

• VP-Operations (Plant Head) at M/s. Swiss Garnier, Sikkim – Led a Rs 500 Mn Greenfield Project for OSD & Topical Solutions
• GM-Project & Engg at M/s. Sarvotham Care, Baddi
• Head-Maintenance & Engineering at Vaccine Manufacturing Co., Chennai
• Head-Engineering at M/s. Shelys Pharmaceuticals, Tanzania – Managed US$11 Mn Greenfield Project
• GM-Projects at M/s. Apex Engineering Services, Nasik – Specialized in HVAC & Clean Room projects

N. Murugesan’s expertise spans across engineering, project execution, and commissioning of pharmaceutical manufacturing plants, delivering projects on time and within budget while ensuring compliance with industry standards.

Vijay Bhusare

GMP Senior Consultant

Vijay Bhusare

GMP Senior Consultant

With over 30 years of experience in pharmaceutical quality management, Mr. Vijay Bhusare specializes in GMP compliance, regulatory inspections, and the implementation of quality systems for pharmaceutical manufacturing organizations. He is highly skilled in guiding and training teams to ensure successful regulatory inspections and the development of robust internal quality standards.

Key Expertise:

• GMP Compliance and Pharmaceutical Quality Management
• Internal & Supplier Quality Auditing
• Regulatory Inspection Preparation (WHO, US FDA, EU, MHRA, PICs)
• Training & Team Development in GMP & Quality Practices

Key Roles:

• General Manager – Head of Quality at Centaur Pharmaceuticals Ltd.
• Site Head Quality Control/Assurance at IPCA Laboratories Ltd.
• Worked with leading organizations like Lupin Ltd, Wockhardt Ltd, Ranbaxy Ltd, Sun Pharma Ltd, and Strides Arco Lab Ltd in various quality management roles.
• Extensive international experience in the Middle East and South East Asia, especially trained by Shimadzu Co., Kyoto, Japan.

Bhusare’s leadership in GMP practices and regulatory compliance ensures that manufacturing operations meet the highest industry standards.

Mithilesh Narendra Trivedi

Sr. Consultant – GMP

Dr. Mithilesh Narendra Trivedi

Sr. Consultant – GMP Ph.D. in Organic Chemistry

With over 38 years of experience in Research & Development, Production, Quality Control, and Quality Assurance, Dr. Mithilesh Trivedi has extensive expertise across Chemicals, Fine Chemicals, Bulk Drugs (API), and Formulation Industries. He is highly skilled in product development, process optimization, and vendor qualification, having audited numerous manufacturing sites globally, including more than 20 in China and several in India.

Key Expertise:

• GxP Operations & Regulatory Compliance
• Product Development & Process Optimization
• Vendor Audits & Supplier Technical Assurance
• Sterility, Pyrogen (LAL Test), and Toxicity Testing
• Training in Quality Control and Assurance
• Documentation & Record Maintenance

Career Highlights:

• Sr. Research Fellowship awarded by the Department of Science and Technology, Government of India
• Council Member of Indian Pharmaceutical Association (IPA), Maharashtra State Branch
• Vice Chairman for the Technical Sub-Committee and Committee Member of the R&D Sub-Committee of IDMA
• Elected as Founder President of IPA, Bhiwadi Local Branch
• Recognized with multiple appreciation certificates by various government departments in Uzbekistan

Dr. Trivedi’s wealth of experience ensures his ability to drive quality improvements, regulatory compliance, and efficient vendor management in complex pharmaceutical operations.

Prema

GMP Consultant

Prema

GMP Consultant M.Pharm (Gold Medalist)

Ms. Prema is a Gold Medalist in M.Pharm with extensive experience as a GMP Quality Operations Consultant. She specializes in GMP compliance and practices for pharmaceutical manufacturing organizations, developing tailored technical and quality strategies for different situations. She has a strong background in various dosage forms and is a proficient team leader in both internal and supplier quality auditing.

Key Expertise:

• GMP Compliance & Quality Operations
• Internal & Supplier Quality Auditing
• Regulatory Inspections (WHO, USFDA, MHRA, ANVISA, PICs)
• Internal Quality Standards Implementation
• Team Training and Development

Career Highlights:

• Worked with Navamin Pharmaceuticals, Softgel Healthcare, Saimirra Innopharm, Archimedes Healthcare, and Intermed.
• Highly experienced in guiding and training teams for successful regulatory inspections, ensuring adherence to global regulatory standards.

Prema brings her deep expertise to ensure pharmaceutical companies meet the highest standards in quality management and regulatory compliance.

Velappan

GMP Consultant

Velappan

GMP Consultant B. Sc. Chemistry

Mr. Velappan is a seasoned professional with over 35 years of experience in Quality Control (QC) and Quality Assurance (QA). He has held key positions at prestigious companies such as Medopharm, Central Drugs & Pharma, and Phoenix Laboratories, where he played a pivotal role in driving growth and success.

Key Expertise:

• Quality Control (QC) & Quality Assurance (QA)
• Audit Management for International Regulatory Bodies
• Global Regulatory Compliance
• GMP Audits for MHRA, WHO, and various African Health Authorities

Career Highlights:

• Extensive audit experience with MHRA (UK), WHO-GMP, and other regulatory bodies in Africa (Kenya, Uganda, Zimbabwe, etc.), as well as UNICEF and USAID.
• Trusted expert in conducting audits for key international organizations such as NDA, NAFDAC, and Médecins Sans Frontières (MSF).

Velappan’s expertise in audits and compliance ensures that pharmaceutical organizations maintain the highest standards of quality assurance across global markets.

Iyyappan

GMP Consultant

Iyyappan

GMP Consultant Masters in Chemistry, Diploma in Instrumentation (DCPIC), Drug Regulatory Authority (DRA), PGDCA (Computer Application)

Iyyappan is an experienced GMP Consultant with over 15 years of expertise across multiple areas, including Quality Control (QC), Quality Assurance (QA), Regulatory Compliance, and Software Validation. His background spans several aspects of pharmaceutical operations, including product release, validation, and regulatory affairs.

Key Expertise:

• Quality Control (QC) & Quality Assurance (QA)
• Regulatory Affairs (Dossiers, Submissions, Audit Handling)
• Qualification & Validation (including Computer System Validation – CSV)
• Good Laboratory Practices (GLP) and Quality Management Systems (QMS)
• Risk Management (QRM)
• Product Release (Tablets, Capsules, Oral Liquids)

Achievements:

• Expertise in handling audits from US FDA, ANVISA, MHRA, and WHO-Geneva.
• Awarded Best Trainer at Sun Pharma and Won a prize in the Go Lean Management Competition to save costs and improve productivity.

Iyyappan is well-versed in preparing dossiers, protocols, and SOPs, ensuring pharmaceutical companies meet regulatory compliance while driving quality improvements and operational efficiency.

Srinivasa Rao

GMP Consultant

D. Srinivasa Rao

GMP Consultant M.Pharma, PG Diploma in Business Management

Mr. D. Srinivasa Rao is a seasoned GMP Consultant with 34 years of experience in the pharmaceutical industry, specializing in the manufacturing of pharmaceutical formulations. He has held both technical and management positions at reputed pharmaceutical organizations, with a focus on tablets, capsules, and topical dosage forms.

Key Expertise:

• Production Experience with leading pharmaceutical organizations.
• Plant Administration and Project Management.
• GMP Audits for domestic, ROW, and regulated markets (including EU GMP).
• ISO 9001:2015, QMS, and ISO 22000 QMS management.
• Strong administrative, technical, and troubleshooting skills.
• Excellent communication skills and adaptability to diverse work environments.

Rao’s versatility and expertise in handling audits and project management make him a valuable asset in ensuring compliance and enhancing the quality of pharmaceutical operations.

Joseph Sahaya Raj

GLP & Analytical Consultant

Joseph Sahaya Raj. R

GLP & Analytical Consultant B. Pharma

Joseph Sahaya Raj. R is a highly experienced GLP & Analytical Consultant with over 30 years of expertise in Quality Control and Quality Assurance. He has contributed significantly to renowned pharmaceutical organizations such as Tablets India Ltd., Shasun Chemicals & Drugs Ltd., Indo French Laboratories, Caplin Point Laboratories, Dr. Milton Laboratories, Micro Therapeutic Research Ltd., and Azidus Laboratories Ltd..

Key Expertise:

• Over 30 years of experience in Analytical Sciences and Quality Assurance.
• Research & Paper Publication experience, with contributions to top journals like:
• IOSR Journal of Pharmacy
• Journal of Chromatography & Separation Techniques
• International Journal of Advanced Research
• Pharmaceutical Investigation & Research
• Specialized in drug development, research, and clinical research.

His deep knowledge and experience in analytical methods and research publications make him a key figure in pharmaceutical analytical consulting.

Viswanatha Sharma

Licensing Consultant

Viswanatha Sharma M.

Licensing Consultant B. Pharma

Mr. Viswanatha Sharma M. is a seasoned Licensing Consultant with over 30 years of experience in project coordination and pharmaceutical manufacturing. He has a strong background in working with renowned companies like Sara Life Science and other pharmaceutical manufacturing organizations.

Key Expertise:

• Manufacturing of Tablets & Liquid Orals
• Project Planning & Execution: Extensive experience in planning, production control, and monitoring within budgetary limitations and time constraints.
• Quality Control/Inspection: Expertise in ensuring adherence to ISO 9000, GMP, and FDA standards.
• Equipment Maintenance & Calibration: Skilled in maintenance and calibration of equipment.
• Certification and Regulatory Compliance: Certified in ISO 9000, Ministry of Health, Quality of Life, and GMP & FDA.

His extensive experience in manufacturing, quality control, and project management makes him a valuable consultant in the licensing and regulatory compliance areas.

Lalit Kumar

GMP Consultant –Medical Devices

Lalit Kumar

GMP Consultant –Medical Devices PGSM, Lean Six Sigma – MBB, BB & GB

Mr. Lalit Kumar is a seasoned GMP Consultant with over 12 years of experience in Project Management, Process Engineering, and Lean Six Sigma. He holds expertise in tooling development, new product introduction, design & process validation, and budgeting.

Key Expertise:

• Lean Six Sigma: Expertise in Business Excellence, Operation Excellence, and Process Excellence.
• New Product Development: Skilled in SPM Automation and new product introductions.
• Project Management & Process Engineering: Specialized in validation of design & process and tooling development.
• Consulting Experience: Worked with reputed companies such as Henry Harvin Education, Polymedicure Limited, Indication Instruments Limited – Veethree, Biotech Vision Care Pvt. Ltd., and Super Auto India Ltd..

With his in-depth knowledge of Lean Six Sigma and operational excellence, Mr. Lalit Kumar brings valuable insights into process improvement and new product development.

Manivannan

Clean Room & Project Consultant

A. Manivannan

Clean Room & Project Consultant

Industry Expert in Pharmaceutical and Medical Devices Regulatory Compliance and Engineering Solutions

Mr. A. Manivannan brings over 30 years of extensive experience in project planning, execution, qualification, validation, and engineering solutions tailored for pharmaceutical and medical device manufacturing industries. His expertise lies in aligning facilities and processes with global regulatory standards such as cGMP, USFDA, EU GMP, ANVISA, and MDD to MDR (India & EU) conversions.

Professional Journey:

• Star Drugs & Research Labs Private Limited: Contributed to engineering and regulatory initiatives.
• Straights Acrolab: Enhanced operational efficiencies.
• Caplin Point Laboratories Private Limited: Led regulatory compliance projects.
• Dexin Medi Solutions Private Limited: Provided expert consultancy services for compliance and validation.
• Trustin Analytical Solutions Private Limited: Delivered strategic guidance for analytical and validation projects.
• Dexin Medi – Clarus Solutions: Currently heading as CEO, offering consultancy services focused on regulatory readiness and operational optimization.

With his deep knowledge of regulatory compliance and engineering solutions, Mr. Manivannan has significantly contributed to enhancing operational efficiency and regulatory alignment across the pharmaceutical and medical device industries.

Gopalsamy

Principal Consultant – Analytical & GLP

P. Gopalsamy, M.Sc. Chemistry

Principal Consultant – Analytical & GLP

Professional Profile

With a distinguished career spanning 35 years, Mr. P. Gopalsamy has demonstrated exceptional expertise in Quality Control, Analytical Research & Development, and leadership as a Head of Department. Key areas of specialization include:

• Good Laboratory Practices (GLP): Extensive experience in GLP activities, ensuring compliance and maintaining rigorous quality standards.
• Compliance and Validation: Expertise in qualification, validation, material handling, product release, and stability management.
• Troubleshooting: Proven ability to efficiently identify and resolve technical issues.
• Administrative and Technical Leadership: Strong administrative capabilities and robust technical skills, adaptable to various working environments.

Professional Experience

Mr. Gopalsamy has significantly contributed to the following leading organizations:

• Chemplast
• Spic Agri Input Diagnostic Center
• Spic Pharma
• Shasun Pharma
• Strides Pharma
• Solara Pharma

His extensive experience in analytical testing, GLP compliance, and quality assurance has greatly benefited the pharmaceutical industry, ensuring high standards of product quality and regulatory compliance across multiple organizations.

Balakrishnan

Sr. Consultant – Project

B. Balakrishnan, B.Sc. Chemistry

Sr. Consultant – Project

Professional Summary

With over 33 years of extensive experience in the pharmaceutical industry, B. Balakrishnan has built a remarkable career managing complex projects in highly dynamic environments. His strong academic background in science, combined with exceptional managerial skills, has made him a trusted expert in formulation development, regulatory compliance, and production across a wide array of dosage forms and therapeutic areas. Renowned for his analytical and problem-solving abilities, Balakrishnan thrives in deadline-driven settings, consistently delivering high-quality results.

Credentials and Endorsements

• Endorsed by: Tamil Nadu Drug Control Board
• Endorsed Sections:
• Small Volume Parenterals (SVP)
• Safe Parenterals
• IV Fluids
• Oral Dosage Forms

Professional Experience

Balakrishnan has held significant positions in various esteemed organizations, where he has driven growth and ensured operational excellence. His professional journey includes notable companies such as:

• Mediclone Healthcare Pvt. Ltd., Chennai
• MAGNA LABS (Guj.) Pvt. Ltd.
• APOLLO Saline Pharmaceuticals
• Safe Parenterals Pvt.
• Alfred Berg and Company
• Chemech Laboratories
• AKUMS Drugs and Pharmaceuticals
• RUSAN Pharma Ltd.

Throughout his career, Balakrishnan has successfully navigated the complexities of pharmaceutical operations, contributing to the development of cutting-edge projects and ensuring the highest standards of quality and compliance.

Anitha Annamalai

Quality Assurance

Anitha Annamalai, M.Pharm

Quality Assurance

Anitha Annamalai M.Pharm., Post Graduate Diploma in Patent Law, have 13 years of experience in the pharmaceutical industry, specializing in [Formulation Development/Technology Transfer/Production/Quality Control and Quality Assurance.

Have worked with below mentioned companies

- Intermed Laboratories Pvt Ltd, Porur
- Apex Laboratories Pvt Ltd.,(R&D),IKKT
- Shasun Pharmaceuticals Pvt Ltd., Puducherry
- Ajanta Pharma Limited, Kandiveli, Mumbai
- The Madras Pharmaceuticals Pvt.,Ltd.,Chennai
- The Madras Industrial Co-Operative Analytical Laboratory (MICAL),Chennai

Developed and maintained Quality Management Systems (QMS) for continual improvement. Ensured ALCOA+ (Attributable, Legible, Contemporaneous, Original, Accurate) principles for data integrity.

Managed and reviewed Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and Master Documents,SOP’S,QAP’S,

In my 13 years of experience, I have led regulatory audits, improved QMS compliance, and optimized validation processes to enhance product quality. I played a key role in ensuring regulatory approvals, reducing deviations, and mentoring teams to maintain a strong quality culture. Additionally, I worked on process improvements that reduced batch failures and increased efficiency in production.

Kalyanasundaram

GMP trainer, Auditor & GAP analysis

Kalyanasundaram, M.Sc. Chemistry

GMP trainer, Auditor & GAP analysis

Mr. Kalyanasundaram, M.Sc in chemistry, a highly motivated and experienced professional with more than 30 years experience in API manufacturing, Formulation industry experience with a proven track record in process optimization, Product quality, safety & integrity, quality control, R&D knowledge, Regulatory and prime customer compliance.

GMP trainer, Auditor & GAP analysis consultant and expertise scope for all regulatory agencies.

Problem solving, effective Communication skills (written and verbal), Team building with softskill , Leadership, Analtical skills conducting through analysis of Pharma operation including R&D tech transfer and scale up support, offering recommendations to improve efficiency and ensuring compliance with deep understanding of industry standards and regulations & assisting development and implementation of new pharmaceutical products and stay updated on the latest advancements in pharma field.

Guruprasad

cGMP maintaining

A. Guruprasad., M. Sc. Chemistry & Diploma in industrial Safety

cGMP maintaining

Over the span of 37 years, Guruprasad built a diverse and rewarding career in industries. His journey has taken through various roles in production such as Officer, In-charge and Section Head.

Hazard identification and risk control measures, 5-S implementation, all production activities, cGMP maintaining, production documents and SOP review. All documents maintaining as per various audits. BMR record maintaining, monitor and control, all process parameters with quality and efficient preparation of all documents, reports and yield calculations.

SOP were followed in plants perfectly. Daily reports to management, ensuring safety in all production and maintenance activities. Strong administrative and technical skills. Highly versatile to any working environment. Good performance shown in trouble shooting.

Industrial experience gained in Industries and chemicals, Ultra Marine & Pigments Ltd, Malladi drugs, Spic Pharma, Nutra’s Specialities, Narasimma Petro Products and Pioneer Jellice India Private Ltd.

Rabinson Thiviyanathan

Contract Research and Manufacturing Services

Rabinson Thiviyanathan, M.Sc, M.Phil , MBA.

Contract Research and Manufacturing Services

Rabinson Thiviyanathan is a pharmaceutical quality expert with rich years of experience in Quality Assurance/Control, Technology Transfer and Contract Research and Manufacturing Services (CRAMS) for handling of various categories of Molecules.

He is very conversant in the recent development and requirements of with regulatory agencies and has good experience of handling various regulatory inspection like USFDA, MHRA, EU-GMP, WHO-GMP, TGA and PMDA.

He worked at

Merck India Limited,
Sun Pharmaceutical Industries Limited,
Wockhardt Limited
Excel Industries Limited
Solara Active Pharma Sciences Limited.

Inactive

Inactive

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Advisory Team

Merugu Raju

Principal Consultant

Rajendraprabhu

Sr. Consultant – Biotechnology Projects

Sudesh Kumar

Sr. Consultant – HVAC & Clean Room Solutions

Sanjay Shukre

Sr. Consultant – Projects Management

Samir Vasavada

Sr. Consultant – Pharma Operations

Sunil Kanvinde

Sr. Consultant – Life Science Management

Yuvaraj

Principal Consultant – Clinical Research

Murugesan

Sr. Consultant Projects & Engineering

Vijay Bhusare

GMP Senior Consultant

Mithilesh Narendra Trivedi

Sr. Consultant – GMP

Prema

GMP Consultant

Velappan

GMP Consultant

Iyyappan

GMP Consultant

Srinivasa Rao

GMP Consultant

Joseph Sahaya Raj

GLP & Analytical Consultant

Viswanatha Sharma

Licensing Consultant

Lalit Kumar

GMP Consultant –Medical Devices

Manivannan

Clean Room & Project Consultant

Gopalsamy

Principal Consultant – Analytical & GLP

Balakrishnan

Sr. Consultant – Project

Anitha Annamalai

Quality Assurance

Kalyanasundaram

GMP trainer, Auditor & GAP analysis

Guruprasad

cGMP maintaining

Rabinson Thiviyanathan

Contract Research and Manufacturing Services

Inactive

Services

Business Challenges

Project Service

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Biopharmaceuticals

Project Service

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