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Our Company

Having started operations in 1996, we have two decades of experience sustaining relationships with large pharma companies by delivering quality sterile products for the Indian market.

We are a company that specializes in Sterile Injectables. Our manufacturing facility has USFDA and EU GMP approvals. We manufacture sterile solutions in vials and ampoules and will have lyophilization capability by March 2021.

Right from inception, we have built a reputation as a reliable supplier and partner for sterile injectables Contract Manufacturing. As we extended our presence in North America, Europe and Australia, we have gained recognition for our Quality, Compliance and Ethical Business practices.

We provide services to various regulated markets viz. US, Europe, Canada and Australia, etc. Our services include:

    • Product Development and Commercial Supply (CDMO)
    • Technology Transfer for Commercial Supply, and
    • Product Licensing.

We have the capability to partner with you from Development to Commercial Supply.

Our facility which is located in Hosur, Tamilnadu (India), which is 44 miles (70 Km) south of Bengaluru International Airport and 193 miles (310 Km) east of Chennai Port.  The facility is spread across 5 acres. 

Our Team

Leading the Organisation Ahead

Dr. Bhaskar Krishna

Managing Director and Chief Executive Officer

In 2013, Dr. Krishna became part of Maiva Pharma (then Global Pharmatech) as Promoter/Managing Director/CEO. With conviction in the company’s intrinsic potential, its quality systems and processes, Bhaskar spearheaded the company’s entry into regulated markets such as Canada, European Union, and Australia. This facilitated acceleration in the inspection process by Health Canada, followed by EU inspection and approval. This was quickly followed by PIC/S approval by Malaysia.

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Mr. Shivananda Hegde

CFO and Company Secretary

Shivananda Hegde joined Maiva in 2007. He had played varied roles in our organization from Financial Controller to Company Secretary. Currently, in addition to his responsibilities as CFO and Company Secretary, Hegde also heads Human Resource.

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Dr. Alagumurugan Alagarswamy

VP & Head - Research & Development

Dr. Alagu, heads Research & Development and Technology Transfer. He has over 20 years of experience in Pharmaceutical industry. Dr. Alagu had filed 70+ ANDAs in a broad range of categories notably in Injections (i.e.  Liquid injections, Lyo formulations, Liposomal and Suspensions), Nasal Sprays and Inhalation solutions.

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Mr. Arul Prasadh

AVP-Operations

Arul Prasad, AVP heads Operations. Arul has over 20+ years experience in the Pharmaceutical Industry. Arul has handled various delivery formats in sterile manufacturing including Ampoules, Vials, Lyophilized products, PFS and Bags. He has extensive experience in setting up new capabilities, new line additions and has handled numerous tech transfer projects to his credit. Arul oversees day-to-day operations and brings in efficiency by implementing Operational Excellence concepts.

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Mr. Chezhian

AVP-Quality Operations

Mr. Chezhian heads Quality Operations for Maiva.  He has been with Maiva for over 22+ years. He leads all the quality functions within Maiva and support them. Chezhian gained hands on experience in Quality Control and Quality Assurance before heading Quality Operations. He had handled international regulatory audits viz. USFDA, EU-GMP, TGA-Australia, PIC/S and Health Canada and multiple customer audits.

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Mr. Viswanathan

VP-Supply Chain

Viswanathan, VP Supply Chain, leads Maiva’s Supply Chain division. He has 25+ years of experience in managing supply chain. Over the years, he had been the person leading efforts to upgrade capabilities of Maiva’s supply chain. His efficient planning, productivity, optimized resource utilization and customer relationship management have contributed to Maiva’s growth.

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Mr. Mahantesh Wali

Head - Regulatory

Mahantesh Wali has over 15 years of experience in the field of Global Regulatory Affairs, Regulatory Strategy, Regulatory compliance and Pharmacovigilance. He has expertise in Regulatory Filing of Sterile formulations (Peptide formulations, Low Molecular Weight Heparins, Anticoagulants, Combination products, Ophthalmics, LVPs in flexible bags and Oncology molecules) for Various markets VIZ US, EUROPE, CANADA, AUSTRALIA, CHINA regions.

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Mr. Sellaraj Pandiyan

Head - Business Development

Sella heads Maiva’s Business Development division, with responsibilities in Delivery, Account Management, Alliance and Portfolio Management. He has more than 15+ years of experience in the Pharmaceutical Industry spanning across Technical Services, Project Management and Business Development.

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