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फार्मास्युटिकल अनुसंधान

फार्मास्युटिकल अनुसंधान

Brief overview:

The Ayurvedic medicines are broadly classified into 2 categories viz. i) classical Ayurvedic medicines which are manufactured in accordance with the formulae described in authoritative books of Ayurveda as specified in the First Schedule of Drugs & Cosmetics Act 1940, Rule 1945 and ii) Patent or proprietary Ayurvedic medicines which are manufactured containing ingredients mentioned in authoritative books of Ayurveda as specified in the First Schedule but not administered by parenteral route and also formulation not included in the authoritative books.

CCRAS undertakes research to validate classical Ayurvedic formulations and scientifically validate new formulations/drugs. Under validation of classical Ayurveda formulations, the Council has identified classical Ayurveda formulations for identified disease conditions, referring to Ayurvedic pharmacopeia /Ayurvedic Formulary of India, Essential Drug list of ASU medicines, Ministry of Ayush, and other Ayurveda classical texts. These quality-assured classical formulations are being validated through the Council’s institutes. Further, the Council develops standards for the classical Ayurved medicines for which API standards are not available.

The Council undertakes drug development in diseases of national importance through systematic process of drug development viz. drug standardization and quality control, preclinical safety/toxicity studies and biological activity studies (as appropriate) and clinical trials as per requirement. These Ayurvedic drugs are made available into the healthcare system through transfer of technology through NRDC.

Details of the scheme and objectives: The CCRAS- Drug Development Cell was set up during the year 2017-18. This cell has been reconstituted as a Product development and trial drug coordination cell with effect from 22रा August 2023, with the following terms of reference:

  • Co-ordination of product development, liasoning with concerned programme officers and scientists of various disciplines.
  • Appraisal of ongoing Research regarding various stages of product development, such as standardization, including Pharmacognosy, Phytochemistry, Stability, Preclinical, safety, efficacy, and Mechanistic studies, and Clinical studies.
  • Liasoning and coordination of development of Dossier in Coordination with Translational Research, Intellectual Property Rights, and Business Development (TRIPR & BD) Cell.
  • Identification of Gaps based on various ongoing and completed studies and available leads in the chain of product development
  • Coordination for Randomization of trial drugs and ensuring the availability of drugs for Clinical studies as per requirement
  • Coordination and liasoning for ensuring the supply of trial drugs by the Nodal Officer/PI in coordination with TRIPR & BD cell.
  • Coordination with the Pharmaceutical industry and PCIM&H for product development issues.
  • Media Management and IEC activities related to Drug development.

Core Objectives:

  • To undertake research studies for the  development of SOP of Classical and New Dosage forms of Ayurvedic medicines.
  • Pharmaceutical Standardisation of formulations as per API/AFI guidelines and Classical Ayurvedic texts.
  • Preparation of formulations as per API/AFI guidelines and Classical Ayurvedic texts.
  • Establishment of Quality control parameters for Ayurvedic drugs
  • Development of new products and technology transfer to industries
  • Preparation and supply of trial drugs for various research projects
  • Preparation and supply of medicines for OPD and IPD of the CCRAS institutes.

Scientist working:

CCRAS -Headquarters

  1. Dr. T. Maheswar, Assistant Director (Ayurveda)
    1. Dr. B S Sharma, अनुसंधान अधिकारी (आयुर्वेद)
    1. Dr Shruti Khanduri, अनुसंधान अधिकारी (आयुर्वेद)
    1. Dr Mukesh Chincholikar, अनुसंधान अधिकारी (आयुर्वेद)
    1. Dr Rohit K.S., Research Officer (Ayurveda)
    1. Dr.Varsha Sumedan, Research Officer (Ayurveda)

CCRAS Peripheral Institutes involved:

  • केंद्रीय आयुर्वेद अनुसंधान संस्थान, झाँसी
  • केंद्रीय आयुर्वेद अनुसंधान संस्थान, भुवनेश्वर
  • केंद्रीय आयुर्वेद अनुसंधान संस्थान, कोलकाता
  • केंद्रीय आयुर्वेद अनुसंधान संस्थान, पटियाला
  • Central Ayurveda Research Institute, Mumbai
  • केंद्रीय आयुर्वेद अनुसंधान संस्थान, नई दिल्ली
  • National Ayurveda Research Institute for Panchakarma – Cheruthuruthy
  • कैप्टन श्रीनिवास मूर्ति केंद्रीय आयुर्वेद अनुसंधान संस्थान, चेन्नई
  • क्षेत्रीय आयुर्वेद अनुसंधान संस्थान, ग्वालियर
  • क्षेत्रीय आयुर्वेद अनुसंधान संस्थान, गंगटोक
  • क्षेत्रीय आयुर्वेद अनुसंधान संस्थान, रानीखेत
  • क्षेत्रीय आयुर्वेद अनुसंधान संस्थान, मंडी
  • क्षेत्रीय आयुर्वेद अनुसंधान संस्थान, जम्मू
  • क्षेत्रीय आयुर्वेद अनुसंधान संस्थान, जयपुर
  • क्षेत्रीय आयुर्वेद अनुसंधान संस्थान, लखनऊ
  • Regional Ayurveda Research Institute,  Patna
  • Regional Ayurveda Research Centre, Dimapur
  • Regional Ayurveda Research Centre, Agartala
  • Regional Ayurveda Research Centre, Trivandrum

Infrastructure and Facility-Based Informational

CCRAS has 5 GMP-certified pharmacies at Central Ayurveda Research Institute, Jhansi, Central Ayurveda Research Institute, Bhubaneswar, Central Ayurveda Research Institute, Kolkata, Central Ayurveda Research Institute, Patiala and National Ayurveda Research Institute for Panchakarma, Cheruthuruthy with sophisticated instruments in different sections, viz. Churna, Tablet, Capsule, Taila, Ghrita, Avaleha, and Rasaushadhis. These pharmacies are associated with well-equipped Quality control labs.

  • State-of-the-art, sophisticated facilities in each section are well equipped with instruments.
  •  Advanced tools enable cutting-edge research in Ayurveda.
  • The availability of such instruments facilitates accurate and precise data collection and analysis..
  • Various sections under one umbrella ie Ayurveda Research Pharmacy, Botany, Pharmacognosy, Chemistry, Microbiology Section and Pharmacology Section.

Rasaushadhi Section

HI
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