Ayush Siddha Manufacturing License
Obtaining an Ayush Siddha manufacturing license is essential for legally producing Siddha medicines in India. The process involves registering with the Ministry of AYUSH, ensuring compliance with Good Manufacturing Practices (GMP), and submitting necessary documentation such as proof of registration, manufacturing unit details, and product formulations.
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Siddha word came from a Tamil word which means perfection or achievement. Originating from South India, it is an ancient system of medicine and healing. As per popular belief, the Siddha system of medicine is divine in origin.
The treatment is aimed at restoring balance to the mind-body-spirit system. Siddha lays equal emphasis on the body, mind, and spirit and strives to restore complete harmony to the various psychological and physiological functions of the body. In Ayurveda, yoga, meditation, diet and lifestyle (pathya and apathya) play a major role in correcting body-mind balance, curing diseases, and maintaining health. Kayakarpam, Varmam, and Thokkanam are the main therapies used in Siddha.
This system of medicine places more importance on preventing diseases than curing them known as Pini Anugaa Vidhi.
The remedies recommended by Siddha have been verified through scientific research. It is accepted to be highly effective in treating diseases of the:
- Skin,
- Liver, and
- Prostate
It is believed to be one of the oldest forms of medical practice in the world. Siddha advocates living in harmony and balance with the nature around us with a focus on diet, lifestyle, and exercise. By tapping into the benefits of a comprehensive, natural, and harmonious lifestyle with Siddha, one can be assured to be cured of many chronic ailments without producing any side effects.
About AYUSH
The Ministry of AYUSH was formed in 9th November 2014 to ensure the optimal development and propagation of AYUSH systems of health care. Earlier it was known as the Department of Indian System of Medicine and Homeopathy (ISM&H) which was created in March 1995 and renamed as Department of Ayurveda, Yoga and Naturopathy, Unani, Siddha and Homeopathy (AYUSH) in November 2003, which focused attention for the development of Education and Research in Ayurveda, Yoga and Naturopathy, Unani, Siddha, and Homeopathy.
If you are interested in ayurvedic medicine manufacturing, you have to take a license from AYUSH, but if you are only dealing with selling of ayurvedic medicine you don’t require an AYUSH license. Also, for setting up an Ayurvedic clinic and panchakarma center, you need to be a registered Ayurvedic practitioner.
Objectives:
- To upgrade the educational standards of Indian Systems of Medicines and Homeopathy colleges in the country.
- To strengthen existing research institutions and to ensure a time-bound research program on identified diseases for which these systems have an effective treatment.
- To draw up schemes for promotion, cultivation and regeneration of medicinal plants used in these systems.
- To evolve Pharmacopoeial standards for Indian Systems of Medicine and Homoeopathy drugs
Qualifications Required for Siddha Manufacturing License
The manufacturing of Ayurvedic medication must be conducted underneath the direction and oversight of competent technical employees consisting of minimum of 1 person, who is a permanent employee of the company and possesses minimum of any qualification as described below: -
- A Degree in Ayurveda or Ayurvedic Pharmacy, Siddha or Unani systems of medicine from an authorized university or college or;
- A Diploma in Ayurveda or Ayurvedic Pharmacy, Siddha or Unani systems of medicine from an authorized university or college or;
- A graduate in Pharmacy or Chemistry or Botany from a recognized university with experience of minimum 2 years in manufacturing of ayurvedic drugs or;
- A Vaid or Hakim registered in a State Register of Practitioners of medicines having experience of at least four years in the manufacturing of ayurvedic drugs.
- A qualification as Pharmacist in Ayurvedic (including Siddha) or Unani systems of medicine, having experience of at least eight years in the manufacturing of Ayurvedic medicine.
Documents Required for AYUSH Siddha License:
- Incorporation / Proprietary / Other form of business
- Area of manufacturing unit should be not less than 1285 sq. ft.
- DMR Act [The Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954]
- (DMR act compliances must followed by all manufacturers)
- Technical officer
- Product information (what are the product going to be manufacture)
- Form of product [in what form (tablets/liquid/powder) product going to be manufacturing)
- Directors (related to herbal domain) will be more preferable
- GST Certificate
- Aadhaar and PAN Card of Authorized Person
- GMP Certificate
AYUSH Siddha License Registration Steps:
- Connect with Corpseed team
- Submit all the documents required for AYUSH license
- We will verify & complete the documents
- We will draft Affidavit
- We will draft & file the application to Ministry of Ayush.
- Fee payment
- Follows-ups with Ministry of Ayush
- We will send certificate copy to you via email or courier
What is included in Siddha Manufacturing License?
- Free Consultation for Siddha Manufacturing License
- Document Preparation
- Application Drafting AYUSH License
- Application Filing with AYUSH Department
- Payment to Government
- Coordination with the government department
- Obtain AYUSH License and Delivery via Courier & Email
Corpseed Additional Services:
- Documents preparation including all the required affidavits
- Formulation development
- Evaluation of formulation as per drugs license format.
- Consultation for Goods Manufacturing Practice certificate
- Preparation of consumer product report/ leaflet
- Providing textual and research reference for ingredients of the different disease
Connect With Corpseed
Connect with the Corpseed team to discuss your requirements at IVR: 7558640644 or hello@corpseed.com. It takes 20–25 minutes to discuss the requirement.
Dedicated Manager
Once you discuss the requirement, we will align a dedicated Account Manager to understand your business needs and assist throughout the process.
Real Time Update
Track the progress of your application and always know what’s in progress and what’s done.
Job Completed
Once the job is completed, you will receive registrations & certifications directly to your email ID and at your doorstep.
Frequently Asked Questions
Quick answers to common questions about this service.
What is an Ayush Siddha manufacturing license?
It is a license required to manufacture Siddha medicines legally, as per the guidelines of the Ministry of AYUSH.
Why is this license required?
It ensures that the manufacturing process meets quality standards, safety regulations, and legal requirements.
What are the benefits of holding an Ayush Siddha manufacturing license?
It increases credibility, helps to stay within the ambit of law, and gets government schemes and market opportunities.
What is the duration of the application process?
Surprisingly, the process lasts several months, depending on how complete the application might be and the time necessary for inspections.
Can a license be renewed?
Yes, it has to be renewed every year, and the process of renewal is done through the submission of updated documents and compliance reports.
What are the GMP requirements for Siddha medicines?
GMP includes cleanliness, proper documentation, quality control, and regular audits so that one can be assured of following standards.
What is the State Licensing Authority's role in the license process?
The State Licensing Authority checks for applications, examines the places, and cross-verifies that all norms have been followed, and after approval of the State Licensing Authority license is given.
How many times inspection will be conducted by the authority for licensed manufacturing units?
Annual inspection is usually performed to maintain a consistent level of GMP compliance along with other regulatory compliance.
What if a licensed manufacturing unit is failed in the inspection?
Rectification measures might be taken to correct any non-compliance. Non-rectification would result in license suspension or cancellation.
Are there specific labeling requirements for the Siddha drugs?
Yes. The packaging of Siddha drugs should be in compliance with labeling requirements listing ingredients, dosages, cautions, or warnings.
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