India's Premier AYUSH Regulatory Consultancy
Helping Ayurvedic, Siddha, Unani and Herbal Manufacturers achieve regulatory excellence through licensing, product approvals, manufacturing compliance, documentation, R&D and market-ready solutions.
- 25+ Years Experience
- 1000+ Products Developed
- Regulatory Experts
- Manufacturing Consultants
- PAN India Support
AYUSH LICENSE
& WHO GMP
Manufacturing Plant
& Research Lab Setup
Legal Documents
& Digital Compliance
India's Premier AYUSH Regulatory Consultancy
Helping Ayurvedic, Siddha, Unani and Herbal Manufacturers achieve regulatory excellence through licensing, product approvals, manufacturing compliance, documentation, R&D and market-ready solutions.
- 25+ Years Experience
- 1000+ Products Developed
- Regulatory Experts
- Manufacturing Consultants
- PAN India Support
AYUSH LICENSE
& WHO GMP
Manufacturing Plant
& Research Lab Setup
Legal Documents
& Digital Compliance
Industries We Serve
Ayurveda
Unani
Siddha
Homeopathy
Nutraceutical
Cosmetics
Herbal Supplements
Food Products
Personal Care
Industries We Serve
Ayurveda
Unani
Siddha
Homeopathy
Nutraceutical
Cosmetics
Herbal Supplements
Food Products
Personal Care
Our Services
AYUSH Licensing
WHO GMP
Product Approval
Manufacturing Setup
R&D Laboratory
Documentation
Third Party Manufacturing
Import Export
Legal Compliance
Our Services
AYUSH Licensing
WHO GMP
Product Approval
Manufacturing Setup
R&D Laboratory
Documentation
Third Party Manufacturing
Import Export
Legal Compliance
Consulting Process
A streamlined journey from concept to compliance.
Book Appointment
Requirement Analysis
Documentation
Submission
Approval
Support
Consulting Process
A streamlined journey from concept to compliance.
Book Appointment
Requirement Analysis
Documentation
Submission
Approval
Support
Trusted by AYUSH Manufacturers Across India
For over 25 years, Pippli Solutions has partnered with Ayurvedic, Siddha, Unani, Herbal, Cosmetic, and Nutraceutical manufacturers to simplify regulatory compliance, accelerate product approvals, and build successful manufacturing businesses.
Mr. Ramesh Kumar
Managing Director
Ayurvedic Manufacturing Company
Hyderabad, Telangana
Exceptional Regulatory Expertise
"Pippli Solutions guided us through every stage of obtaining our AYUSH manufacturing license. Their documentation, technical expertise, and prompt support helped us establish our manufacturing unit with complete confidence."
Dr. Shalini Verma
Research & Development Head
Herbal Healthcare Pvt. Ltd.
Bengaluru, Karnataka
Outstanding Product Approval Support
"We approached Pippli Solutions for proprietary Ayurvedic product documentation and formulation guidance. Their deep understanding of AYUSH regulations made the approval process smooth and hassle-free."
Mr. Vijay Patel
Factory Director
Natural Wellness Industries
Ahmedabad, Gujarat
Reliable GMP Consultancy
"The team helped us upgrade our facility to meet WHO-GMP standards. Their practical recommendations and regulatory knowledge significantly improved our quality systems."
Mrs. Sneha Nair
Quality Assurance Manager
Ayush Care Laboratories
Kochi, Kerala
Professional Documentation Services
"From SOP preparation to validation documents and quality manuals, every document delivered was professionally prepared and accepted during inspections."
Mr. Srinivas Rao
Director
Herbal Formulations Pvt. Ltd.
Vijayawada, Andhra Pradesh
Excellent Manufacturing Plant Consultancy
"Their expertise in plant layout planning, equipment selection, and regulatory compliance saved us considerable time and investment during our factory setup."
Dr. Meera Joshi
Technical Director
Ayurveda Research Centre
Pune, Maharashtra
Trusted Long-Term Regulatory Partner
"Pippli Solutions has been our regulatory consultant for several years. Their support in product registrations, labeling compliance, and legal documentation has been invaluable."
Trusted by AYUSH Manufacturers Across India
For over 25 years, Pippli Solutions has partnered with Ayurvedic, Siddha, Unani, Herbal, Cosmetic, and Nutraceutical manufacturers to simplify regulatory compliance, accelerate product approvals, and build successful manufacturing businesses.
Mr. Ramesh Kumar
Managing Director
Ayurvedic Manufacturing Company
Hyderabad, Telangana
Exceptional Regulatory Expertise
"Pippli Solutions guided us through every stage of obtaining our AYUSH manufacturing license. Their documentation, technical expertise, and prompt support helped us establish our manufacturing unit with complete confidence."
Dr. Shalini Verma
Research & Development Head
Herbal Healthcare Pvt. Ltd.
Bengaluru, Karnataka
Outstanding Product Approval Support
"We approached Pippli Solutions for proprietary Ayurvedic product documentation and formulation guidance. Their deep understanding of AYUSH regulations made the approval process smooth and hassle-free."
Mr. Vijay Patel
Factory Director
Natural Wellness Industries
Ahmedabad, Gujarat
Reliable GMP Consultancy
"The team helped us upgrade our facility to meet WHO-GMP standards. Their practical recommendations and regulatory knowledge significantly improved our quality systems."
Mrs. Sneha Nair
Quality Assurance Manager
Ayush Care Laboratories
Kochi, Kerala
Professional Documentation Services
"From SOP preparation to validation documents and quality manuals, every document delivered was professionally prepared and accepted during inspections."
Mr. Srinivas Rao
Director
Herbal Formulations Pvt. Ltd.
Vijayawada, Andhra Pradesh
Excellent Manufacturing Plant Consultancy
"Their expertise in plant layout planning, equipment selection, and regulatory compliance saved us considerable time and investment during our factory setup."
Dr. Meera Joshi
Technical Director
Ayurveda Research Centre
Pune, Maharashtra
Trusted Long-Term Regulatory Partner
"Pippli Solutions has been our regulatory consultant for several years. Their support in product registrations, labeling compliance, and legal documentation has been invaluable."
Latest Blogs & Insights
Recent Developments in AYUSH Regulatory Compliance in India (2026)
India's AYUSH sector continues to expand rapidly, supported by increasing domestic demand, export opportunities, and government initiatives. As the industry grows, regulatory compliance has become more rigorous, making it essential for manufacturers to maintain robust documentation...
Read ArticleAYUSH Manufacturing License: A Step-by-Step Guide for New Entrepreneurs
Starting an Ayurvedic manufacturing unit involves much more than setting up production equipment. A successful business begins with proper planning, regulatory approvals, and compliance with applicable licensing requirements...
Read ArticleUnderstanding WHO-GMP Certification for AYUSH Manufacturers
WHO-GMP certification demonstrates that a manufacturing facility consistently produces products according to internationally accepted quality standards. Benefits include increased customer confidence, better export opportunities, and improved production efficiency...
Read ArticleProduct Label Compliance for Ayurvedic Medicines
Product labels are legal documents that communicate essential information to consumers and regulators. Common labeling errors include unapproved therapeutic claims, missing license numbers, and incorrect dosage instructions...
Read ArticleCommon Mistakes During AYUSH Manufacturing Unit Inspections
Top observations during inspections often include poor documentation, uncalibrated equipment, and incomplete cleaning records. Regular internal audits, employee training, and preventive maintenance significantly improve inspection readiness...
Read ArticleHow to Prepare Regulatory Documentation for Proprietary Ayurvedic Medicines
Accurate documentation helps reduce regulatory delays. Essential files include product composition, manufacturing formulas, process parameters, raw material specifications, stability data, and label artwork...
Read ArticleThe Growing Importance of Quality Assurance in AYUSH Manufacturing
Quality assurance is becoming a competitive advantage rather than only a regulatory requirement. Modern QA covers incoming raw material inspection, finished product testing, equipment qualification, and deviation management...
Read ArticleExport Opportunities for Indian AYUSH Manufacturers
Indian Ayurvedic products are increasingly reaching international markets. Key success factors include WHO-GMP compliance, consistent product quality, international labeling requirements, and country-specific registration...
Read ArticleDigital Transformation in AYUSH Regulatory Compliance
Digitalization is helping manufacturers improve efficiency while maintaining compliance. Emerging technologies include electronic documentation, AI-assisted document review, digital batch records, and QR-code traceability...
Read ArticleWhat Every AYUSH Manufacturer Should Know About Regulatory Inspections
Preparing throughout the year—not just before inspections—results in smoother regulatory outcomes. Inspectors typically review manufacturing facilities, personnel qualifications, SOP implementation, and Quality Control Labs...
Read ArticleLatest Blogs & Insights
Recent Developments in AYUSH Regulatory Compliance in India (2026)
India's AYUSH sector continues to expand rapidly, supported by increasing domestic demand, export opportunities, and government initiatives. As the industry grows, regulatory compliance has become more rigorous, making it essential for manufacturers to maintain robust documentation...
Read ArticleAYUSH Manufacturing License: A Step-by-Step Guide for New Entrepreneurs
Starting an Ayurvedic manufacturing unit involves much more than setting up production equipment. A successful business begins with proper planning, regulatory approvals, and compliance with applicable licensing requirements...
Read ArticleUnderstanding WHO-GMP Certification for AYUSH Manufacturers
WHO-GMP certification demonstrates that a manufacturing facility consistently produces products according to internationally accepted quality standards. Benefits include increased customer confidence, better export opportunities, and improved production efficiency...
Read ArticleProduct Label Compliance for Ayurvedic Medicines
Product labels are legal documents that communicate essential information to consumers and regulators. Common labeling errors include unapproved therapeutic claims, missing license numbers, and incorrect dosage instructions...
Read ArticleCommon Mistakes During AYUSH Manufacturing Unit Inspections
Top observations during inspections often include poor documentation, uncalibrated equipment, and incomplete cleaning records. Regular internal audits, employee training, and preventive maintenance significantly improve inspection readiness...
Read ArticleHow to Prepare Regulatory Documentation for Proprietary Ayurvedic Medicines
Accurate documentation helps reduce regulatory delays. Essential files include product composition, manufacturing formulas, process parameters, raw material specifications, stability data, and label artwork...
Read ArticleThe Growing Importance of Quality Assurance in AYUSH Manufacturing
Quality assurance is becoming a competitive advantage rather than only a regulatory requirement. Modern QA covers incoming raw material inspection, finished product testing, equipment qualification, and deviation management...
Read ArticleExport Opportunities for Indian AYUSH Manufacturers
Indian Ayurvedic products are increasingly reaching international markets. Key success factors include WHO-GMP compliance, consistent product quality, international labeling requirements, and country-specific registration...
Read ArticleDigital Transformation in AYUSH Regulatory Compliance
Digitalization is helping manufacturers improve efficiency while maintaining compliance. Emerging technologies include electronic documentation, AI-assisted document review, digital batch records, and QR-code traceability...
Read ArticleWhat Every AYUSH Manufacturer Should Know About Regulatory Inspections
Preparing throughout the year—not just before inspections—results in smoother regulatory outcomes. Inspectors typically review manufacturing facilities, personnel qualifications, SOP implementation, and Quality Control Labs...
Read ArticleWhy Choose Pippli
Regulatory Experts
Experienced Formulators
End-to-End Consulting
Fast Documentation
Scientific Support
Industry Knowledge
Why Choose Pippli
Regulatory Experts
Experienced Formulators
End-to-End Consulting
Fast Documentation
Scientific Support
Industry Knowledge
Ready to Launch, License, or Expand Your AYUSH Business?
Whether you are establishing a new manufacturing unit, seeking regulatory approvals, developing innovative formulations, or strengthening GMP compliance, our experts are here to guide you every step of the way.
Ready to Launch, License, or Expand Your AYUSH Business?
Whether you are establishing a new manufacturing unit, seeking regulatory approvals, developing innovative formulations, or strengthening GMP compliance, our experts are here to guide you every step of the way.
Frequently Asked Questions
Everything You Need to Know About Our AYUSH Regulatory Consulting Services
Whether you're planning to establish a new manufacturing unit, develop proprietary products, or navigate regulatory requirements, our experts are here to guide you. Below are answers to some of the most common questions from our clients.
The timeline depends on factors such as the completeness of your documentation, readiness of the manufacturing facility, and the processing schedule of the licensing authority. Proper planning and accurate documentation can significantly reduce delays.
Our team assists you from the initial planning stage through documentation, inspection readiness, and regulatory follow-up to help streamline the licensing process.
Regulatory documentation varies depending on the type of product and the stage of your business. It may include:
- Standard Operating Procedures (SOPs)
- Manufacturing Formulae
- Batch Manufacturing & Packing Records
- Quality Control Documentation
- Product Specifications & Raw Material Specifications
- Equipment Qualification Records & Validation Documents
- Label Compliance Review
- Stability and Supporting Technical Documentation (where applicable)
Pippli Solutions prepares documentation in accordance with applicable AYUSH regulatory requirements and industry best practices.
Yes. We provide technical support for the development of classical and proprietary formulations in Ayurveda, Siddha, and Unani systems, subject to applicable regulatory requirements.
Our formulation services include:
- Product concept development
- Ingredient selection & Formula optimization
- Dosage form selection
- Manufacturing process guidance
- Technical documentation support
- Product standardization guidance
Absolutely. We provide end-to-end consultancy for establishing AYUSH manufacturing facilities, including:
- Plant layout planning & Workflow optimization
- Equipment selection & Utility planning
- GMP-compliant infrastructure guidance
- Quality Control Laboratory planning
- Documentation systems & Inspection preparedness
Our objective is to help you establish an efficient and compliant manufacturing unit.
Yes. Our WHO-GMP consultancy services include:
- Facility gap assessment
- Quality Management System (QMS) guidance
- SOP development & Documentation review
- Internal audit preparation & Personnel training
- Corrective and Preventive Action (CAPA) planning
- Inspection readiness support
These services are designed to help manufacturers strengthen compliance with recognized Good Manufacturing Practices.
Yes. We offer professional consultations through:
- Video meetings
- Phone consultations
- Online document review
- Email support
- Virtual project discussions
This allows clients across India to access expert regulatory guidance without the need for travel.
Yes. We help businesses identify suitable manufacturing partners and provide guidance on:
- Product development
- Manufacturing agreements
- Documentation coordination
- Label review
- Regulatory compliance support
Yes. We review product labels to help ensure they align with applicable regulatory requirements, including:
- Mandatory declarations & Ingredient listings
- Dosage and usage instructions
- Caution statements
- Packaging information
- General compliance with relevant labeling provisions
Yes. We assist manufacturers with documentation and regulatory guidance related to exports, helping them prepare for destination-country requirements and quality expectations.
Booking a consultation is simple:
- Visit the Appointment page.
- Select your preferred consultation type (Online or In-Person).
- Choose a suitable date and time.
- Complete the appointment form.
- Make the consultation fee payment (if applicable).
- Receive confirmation with meeting details.
Frequently Asked Questions
Everything You Need to Know About Our AYUSH Regulatory Consulting Services
Whether you're planning to establish a new manufacturing unit, develop proprietary products, or navigate regulatory requirements, our experts are here to guide you. Below are answers to some of the most common questions from our clients.
The timeline depends on factors such as the completeness of your documentation, readiness of the manufacturing facility, and the processing schedule of the licensing authority. Proper planning and accurate documentation can significantly reduce delays.
Our team assists you from the initial planning stage through documentation, inspection readiness, and regulatory follow-up to help streamline the licensing process.
Regulatory documentation varies depending on the type of product and the stage of your business. It may include:
- Standard Operating Procedures (SOPs)
- Manufacturing Formulae
- Batch Manufacturing & Packing Records
- Quality Control Documentation
- Product Specifications & Raw Material Specifications
- Equipment Qualification Records & Validation Documents
- Label Compliance Review
- Stability and Supporting Technical Documentation (where applicable)
Pippli Solutions prepares documentation in accordance with applicable AYUSH regulatory requirements and industry best practices.
Yes. We provide technical support for the development of classical and proprietary formulations in Ayurveda, Siddha, and Unani systems, subject to applicable regulatory requirements.
Our formulation services include:
- Product concept development
- Ingredient selection & Formula optimization
- Dosage form selection
- Manufacturing process guidance
- Technical documentation support
- Product standardization guidance
Absolutely. We provide end-to-end consultancy for establishing AYUSH manufacturing facilities, including:
- Plant layout planning & Workflow optimization
- Equipment selection & Utility planning
- GMP-compliant infrastructure guidance
- Quality Control Laboratory planning
- Documentation systems & Inspection preparedness
Our objective is to help you establish an efficient and compliant manufacturing unit.
Yes. Our WHO-GMP consultancy services include:
- Facility gap assessment
- Quality Management System (QMS) guidance
- SOP development & Documentation review
- Internal audit preparation & Personnel training
- Corrective and Preventive Action (CAPA) planning
- Inspection readiness support
These services are designed to help manufacturers strengthen compliance with recognized Good Manufacturing Practices.
Yes. We offer professional consultations through:
- Video meetings
- Phone consultations
- Online document review
- Email support
- Virtual project discussions
This allows clients across India to access expert regulatory guidance without the need for travel.
Yes. We help businesses identify suitable manufacturing partners and provide guidance on:
- Product development
- Manufacturing agreements
- Documentation coordination
- Label review
- Regulatory compliance support
Yes. We review product labels to help ensure they align with applicable regulatory requirements, including:
- Mandatory declarations & Ingredient listings
- Dosage and usage instructions
- Caution statements
- Packaging information
- General compliance with relevant labeling provisions
Yes. We assist manufacturers with documentation and regulatory guidance related to exports, helping them prepare for destination-country requirements and quality expectations.
Booking a consultation is simple:
- Visit the Appointment page.
- Select your preferred consultation type (Online or In-Person).
- Choose a suitable date and time.
- Complete the appointment form.
- Make the consultation fee payment (if applicable).
- Receive confirmation with meeting details.