Let's discuss your pharmaceutical manufacturing & formulation goals.
Whether you are exploring third-party manufacturing, requesting a dosage quote, or scheduling a WHO-GMP facility audit, our technical desk responds within 24 hours.
Direct Operations Desk
Active NowCorporate HQ & Manufacturing Plant
Plot 14, Pharma City Industrial Area, Baddi, District Solan, Himachal Pradesh – 173205, India
Get Directions on Google MapsDirect Phone Hotline
+91 98765 43210 (General Lines)
+91 98765 43211 (Contract Manufacturing Desk)
Monday – Saturday: 9:30 AM to 6:30 PM IST
Official Email Channels
Business & Trade: contact@evaronpharma.com
Regulatory Affairs: regulatory@evaronpharma.com
WHO-GMP Manufacturing Hub
Baddi Industrial Zone, Himachal Pradesh
Submit Your Requirement
Select your area of interest and fill out the details. Our technical team will reach out with product catalogs and dosage specs.
Connect directly with specialized business units.
Skip generic hold times and reach technical leads for specific product categories.
Human Healthcare Desk
Third-party manufacturing for tablets, capsules, liquid orals, and sterile injectables for domestic brand owners.
Veterinary & Animal Health
Dedicated production lines for bolus, feed supplements, oral liquids, and veterinary API synthesis.
Exports & Regulatory Affairs
Dossier support (CTD/eCTD format), COPP issuance, and customs compliance for global healthcare markets.
Frequently Asked Questions
Quick answers to common questions about third-party agreements and audit scheduling.
What is the typical lead time for third-party commercial production?
For existing approved formulations, standard production cycles take 3 to 4 weeks from raw material QC release. For new formulation registration or tech transfer, lead time is typically 45 days including artwork approval and stability validation.
What documents are required to initiate contract manufacturing in India?
To begin manufacturing under your brand name, we require: (1) Copy of your Drug License (Form 20B / 21B), (2) GST Registration Certificate, (3) Trademark Registration / Brand Authorization Letter, and (4) Non-Resemblance Certificate for brand names.
How do we schedule a physical or virtual WHO-GMP facility audit?
Facility audits can be scheduled by contacting our Quality Assurance team at least 7 business days in advance. We provide full access to GLP testing labs, HVAC environmental records, and batch manufacturing documentation during audit visits.
Do you assist with COPP (Certificate of Pharmaceutical Product) for exports?
Yes. Our Regulatory Affairs cell prepares complete CTD/eCTD dossiers and applies for State FDA COPP issuance to support your registration in target export markets across Asia, Africa, CIS, and Latin America.
Plan a visit to our Baddi manufacturing plant
Experience our Class 100,000 cleanrooms, GLP analytical laboratories, and automated high-speed packaging lines in person.