Welcome to SRV Taxcon
SRV Taxcon is an emerging brand in Taxation and Accounting Consulting, specializing in services for start-up businesses.
We offer a single-window solution for Registration and License:
- Our in-house team handles over 50 types of business licenses.
- We provide end-to-end services across India.
- Ensuring smooth and continuous adherence to all legal.
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Drug License
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- All Services
- Drug License
Wholesale Drug License
Benefits
Legal Authorization to Trade
Enables lawful distribution of medicines and drugs at wholesale level.Boosts Credibility & Trust
Builds confidence among buyers, retailers, and regulatory authorities.Expansion of Business Scope
Allows sale to hospitals, pharmacies, clinics, and other bulk buyers.Prevents Legal Penalties
Ensures full compliance with health and drug control regulations.Facilitates Business with Government & Private Institutions
Required for participating in drug tenders and institutional supply.
🛠️ Process of Registration
Document Review & Consultation
We assess business readiness and prepare the documentation.Appointment of Competent Person
Assistance in appointing a registered pharmacist or qualified staff.Filing of Application
Submission of license application with local Drug Control Office.Inspection & Liaison
Coordinating inspection with Drug Inspector and compliance.License Approval
Delivery of Drug License post-verification and approval.
Documents Required
Application Form in Prescribed Format
Constitution Documents (Partnership Deed / MOA-AOA)
PAN Card of Company/Proprietor
ID and Address Proof of Proprietor/Partners/Directors
Ownership/Lease Deed of Business Premises
Storage Facility Details (Cold storage if applicable)
Affidavit from a Registered Pharmacist or Competent Person
Educational Qualification Certificate of the Competent Person
Appointment Letter of Competent Person
Photo and Signature of Proprietor/Partner/Director
What You’ll Get
Expert Regulatory Compliance Team
End-to-End Licensing Support
Quick Turnaround & On-time Delivery
Liaison with Authorities on Your Behalf
Transparent Pricing & Online Process
Post-License Renewal & Amendment Support
Frequently Asked Questions
Any individual or company involved in the wholesale distribution of drugs, medicines, or vaccines needs this license.
Yes, you must appoint a qualified pharmacist or a competent person with relevant experience.
Typically, it takes 15–30 working days, depending on documentation and department processing time.
Yes, a secure premises with adequate storage and refrigeration (if needed) is mandatory.
No, the license is issued for a specific premises and jurisdiction. For multiple states, separate licenses are required.
Retail Drug License
Benefits
Legal Compliance
Operate your medical or pharmacy business without legal hurdles.Customer Trust
Enhances credibility and builds customer confidence in your business.Access to Branded Medicines
Enables direct procurement from authorized distributors.Eligibility for Government Tenders
Qualifies your retail pharmacy for state and central drug supply schemes.Avoids Legal Penalties
Ensures full compliance with health and drug control norms.
🛠️ Process of Registration
Consultation & Eligibility Check
Understanding your business model and verifying pharmacist details.Document Preparation
Assistance with compiling and notarizing required documents.Online Application Submission
Filing the application with the Drug Licensing Authority.Drug Inspector Visit
Coordination for premises inspection and verification.License Issuance
Follow-up until approval and delivery of Retail Drug License.
Documents Required
Application Form as prescribed
Constitution Documents (Proprietorship/Partnership/MOA-AOA)
PAN Card and Aadhar Card of Proprietor/Partners/Directors
Proof of Premises Ownership or Rent Agreement
Site Plan of the Retail Shop
Pharmacist Qualification Certificate (Diploma/Bachelor of Pharmacy)
Registration Certificate of Pharmacist with State Pharmacy Council
Appointment Letter of Pharmacist
Affidavit of Full-Time Pharmacist Engagement
Recent Passport-Size Photos
What You’ll Get
Specialized Expertise in Drug Licensing
End-to-End Application Handling
Direct Liaison with Drug Department
Transparent Process & Fixed Fees
Quick Turnaround Time
Post-License Compliance Assistance
Frequently Asked Questions
Anyone with a registered pharmacist and a compliant shop setup can apply.
Yes, a full-time qualified pharmacist registered with the State Pharmacy Council is mandatory.
The process usually takes 15–30 working days, subject to department processing.
No, a Retail Drug License permits physical sale; online operations require additional approvals.
No, the license is location and person-specific. A new application is required for any change.
Drugs Manufacturing License
Benefits
Legal Authorization to Manufacture Drugs
Legitimizes your manufacturing unit for domestic and international markets.Brand Credibility
Boosts trust among healthcare professionals, vendors, and consumers.Eligibility for Government and Institutional Tenders
Enables participation in health department procurements.Market Expansion
Facilitates distribution in retail and wholesale pharma channels.Avoidance of Regulatory Penalties
Ensures full compliance with health ministry regulations.
🛠️ Process of Registration
Initial Consultation & Category Identification
Determining your product type and appropriate license form (25, 28, etc.).Document Compilation & Verification
Assisting in preparation of technical documents and staff compliance.Application Filing
Submission of application with the State/Central Licensing Authority.Inspection & Verification
Coordination with Drug Inspectors for facility inspection and staff interviews.License Approval & Grant
Issuance of the license post successful inspection and documentation.
Documents Required
Company Incorporation Certificate / Partnership Deed
Manufacturing Premises Address Proof and Rent/Lease Agreement
Site Layout Plan and Plant Design
Details of Manufacturing Equipment & Machinery
List of Technical Staff with Qualifications and Experience Certificates
Proof of Qualification and Registration of Competent Technical Staff (CTO)
Affidavit of Non-Conviction under Drugs Act
Environmental Clearance and Pollution NOC (if applicable)
GMP (Good Manufacturing Practices) Compliance Details
Product List and Formulation Details
What You’ll Get
Industry-Specific Regulatory Knowledge
CDSCO and State Drug Control Expertise
Strong Coordination with Drug Inspectors
GMP Compliance Guidance
Transparent & Timely Process Execution
Post-License Regulatory Support
Frequently Asked Questions
Any entity involved in the production of allopathic, ayurvedic, or cosmetic drugs must obtain this license.
Licenses are granted based on the product type — allopathic (Form 25/28), ayurvedic, or cosmetic manufacturing.
Yes, Good Manufacturing Practice (GMP) compliance is mandatory for the grant of a manufacturing license.
Generally valid for 5 years, subject to renewal and ongoing compliance.
Yes, a manufacturing license can include multiple formulations and dosage forms, as long as they’re approved.
Cosmetics Manufacturing License
Benefits
Legal Authorization to Manufacture Cosmetics
Operate a compliant cosmetic production facility within India.Brand Trust & Market Access
Enhances brand reputation and allows nationwide or global distribution.Mandatory for Exports
Essential requirement for exporting cosmetics to international markets.Ensures Quality & Safety
Manufacturing under approved norms ensures product safety and compliance.Avoid Regulatory Penalties
Stay protected from fines or product recalls due to non-compliance.
🛠️ Process of Registration
Consultation & License Categorization
Identifying product categories and types (e.g., skincare, haircare, hygiene products).Document Preparation & GMP Compliance
We assist in drafting and organizing technical documents per regulatory norms.Application Submission
Filing the application with the State Drug Authority for cosmetic license (Form 31).Inspection by Drug Inspector
Site inspection for facility hygiene, infrastructure, and staff qualifications.Grant of License
License is issued upon satisfactory review of all legal and technical compliance.
Documents Required
Company Incorporation Certificate / Partnership Deed
Proof of Premises Ownership or Rent Agreement
Site Layout Plan and Production Area Blueprint
Details of Equipment & Manufacturing Infrastructure
List of Qualified Technical Staff with Experience Certificates
Affidavit of Non-Conviction under the Drugs & Cosmetics Act
Good Manufacturing Practice (GMP) Declaration
Product List with Ingredient Details
No Objection Certificate (NOC) from Pollution Control Board
Water Testing Report (Potable Water Certification)
What You’ll Get
Domain Expertise in Cosmetic Regulatory Compliance
End-to-End Service from Consultation to License Grant
Fast-Track Application Filing & Follow-up
Assistance in Facility Layout Planning & Staff Compliance
Post-License Compliance Support
Frequently Asked Questions
Any entity planning to manufacture cosmetics in India, whether herbal, organic, or synthetic, must obtain this license.
The license is generally valid for 5 years and can be renewed thereafter.
Yes, at least one qualified and experienced person must oversee production operations.
Yes, one license can include multiple cosmetic products if properly approved.
Yes, both principal and contract manufacturers must have valid cosmetic licenses.
Cosmetics Import License
Benefits
Legal Authorization to Import Cosmetics in India
Avoid customs detention and legal complications by complying with CDSCO norms.Quick Market Entry
Enables faster clearance of consignments and seamless distribution.Enhanced Brand Credibility
Establishes your brand as regulatory-compliant and trustworthy.Facilitates Ecommerce & Retail Supply
Required for selling through platforms like Amazon, Flipkart, and retail chains.Mandatory for Commercial Use
Essential for importers, distributors, and foreign brands entering India.
🛠️ Process of Registration
Initial Consultation & Product Categorization
Identifying HS codes and classifying the cosmetic products per Indian guidelines.Document Compilation & Legal Drafting
We assist in drafting Power of Attorney, compiling technical dossiers, and preparing submissions.Application Filing with CDSCO (Form 42)
Submission of product application online through SUGAM portal.Scrutiny & Query Handling
Addressing queries raised by CDSCO officials promptly.Grant of Import License (Form 43)
Once approved, Form 43 is issued, allowing import and sale of cosmetics in India.
Documents Required
Application Form 42 (for each product)
Power of Attorney from the manufacturer
Covering Letter with company details
Product Labels and Pack Inserts
Free Sale Certificate (from country of origin)
Ingredient List with percentage composition
Product Specifications & Testing Methods
Manufacturing License of the foreign manufacturer
Undertaking of Non-Animal Testing
Regulatory Certificates (if applicable: FDA, CE, etc.)
What You’ll Get
CDSCO Registration Specialists
Complete Documentation & Regulatory Filing
Transparent & Hassle-Free Process
Support for Label Compliance & Product Classification
Post-License Advisory on Distribution & Customs
Frequently Asked Questions
Yes, every variant or product requires a separate Form 42 application and approval.
An Indian authorized agent or importer can apply on behalf of the foreign manufacturer.
Typically, it takes 4–8 weeks, depending on documentation accuracy and CDSCO processing time.
No. India prohibits animal-tested cosmetics. A non-animal testing declaration is mandatory.
The license is valid for 3 years unless suspended or cancelled earlier by CDSCO.
Client Testimonials
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Product Manager
Rajeev S.
Frontend Team Lead
Emily D.
Backend Engineer,
Ahmed K.
CTO, TechNova
Sophia R.
Full Stack Developer
John M.
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