Faster Product Approvals Leading to Enhanced Market Access !
In India, traditional drugs include Ayurvedic, Siddha or Unani Drugs and herbal products include phytopharmaceuticals and other plant based products used as medicines. Traditional drugs and herbal products are regulated according to the Drugs and Cosmetics Act and Rules by the Indian regulator – CDSCO. The CDSCO recently released a draft regulation, as an amendment to the Drugs & Cosmetic Rules 1945, which defines and outlines regulations for phytopharmaceuticals (GSR 702 (E) Nov24.11.2013).
Vyomus Consulting is a complete product pipeline development partner for Ayurvedic, Siddha, Unani, Herbal, Phytopharmaceuticals and Homeopathy companies developing and commercializing 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 an India based Authorized 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.,
Vyomus Consulting provides end-to-end Product Registration Services and Authorized Agent Services to all importers and manufactures of veterinary products. 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.
Vyomus Consulting 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 :
- Regulatory Strategy Consulting and Liaison
- Complete Product Life Cycle Management
- Compilation of India specific submission dossiers
- Submission management leading to approvals from ALL Stakeholders
- India Specific Labelling and Patient Information / Instructions for Use leaflets
- Post marketing services including Complaint handling, Adverse incident Reporting & Management and product recall support as part of Product safety reporting, Query management, PSUR Writing & Submission activities
- All statutory Marketing Authorization holder’s requirements
- Act as your India Regulatory Department by Applying and Maintaining required approvals, Prepare and review regulatory submission material for compliance to India legislation etc.,
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