Small Molecules Product Development

FASTER PRODUCT APPROVALS LEADING TO ENHANCED MARKET ACCESS !

Optimus is a complete product pipeline development partner for pharmaceutical and biopharmaceutical companies developing and commercializing complex small-molecule APIs and biologic drug products. From discovery to commercialization, we design, implement and provide “Science Based Optimal Business Solutions” specifically tailored to overcome Therapeutic & Medical Technology based Product Development Challenges.

In general, any regulated product which is to be imported, manufactured, stored, distributed, tested or sold in India, has to be registered with the licensing authority (CDSCO) through various procedures. Products tested or sold in India, could be manufactured locally or can be manufactured outside India but Imported for sale or testing into India. Any manufacturer who wishes to import and market products manufactured outside of India, should register the manufacturing site and the list of products which they propose to import for sale. This Product Registration Process leading to Market Authorisation can be implemented only through the manufacturer’s registered office in India, or their Subsidiary or through an Importer or a India based Authorised Agent.

Also, there is a set procedure of application submission, product testing, registration dossier submission, review and approvals from various stakeholders that are required to facilitate Product Approval / Market Authorisation. The approvals are usually in the form of No Objection Certificates/Letters, Approval Letters, Licences etc.,

Optimus provides end-to-end Product Registration Services as well as Authorised Agent Services to all importers and manufactures of small molecules. This end-to-end service offering will help you import, manufacture, test, conduct clinical trials and distribute your products in India (Market Authorisation), efficiently so as to achieve faster product approvals leading to enhanced access to Markets and Opportunities.

This service offering includes Product Testing, Vendor Identification & Management, various stakeholder regulatory submissions, approvals management, independent audit, regulatory reporting, regulatory dossier review and submission to the regulator.

Optimus senior practitioners have a unique blend of business, domain, technology and pharma process outsourcing expertise and include former senior executives from top Pharma, Biotechnology, Clinical Development companies, top tier consultancies, Fortune 500 enterprises, and leading outsourcing service providers. Our team consists of experts in product development, regulatory affairs, pharmacology, toxicology, preclinical and clinical trial design and evaluation, biostatistics, each with extensive product development experience.

We are thus able to provide regulatory consulting and product development services through all stages of product development to enhance the probability of success and achieve faster product approvals leading to enhanced access to Markets and Opportunities.

Our services include the following :

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