Human Healthcare Desk
Third-party manufacturing for tablets, capsules, oral liquids, and sterile injectables for domestic and PCD pharma brand owners.
Technical & Commercial Desk
Contact Evaron Pharmaceuticals
Have inquiries regarding third-party contract manufacturing, formulations, or facility audits? Connect directly with our WHO-GMP certified manufacturing plants across Haridwar (Units I & II, Uttarakhand) & Aligarh (Unit III, Uttar Pradesh) or submit your dosage requirements below.
Submit Your Requirement
Fill out your details below and our technical desk will get back to you with dosage catalogs, pricing, and timelines within 24 hours.
Department Directory
Specialized Business Desks
All inquiries are centralized through our corporate desk and routed to corresponding plant leads across Haridwar (Units I & II) and Aligarh (Unit III).
Veterinary & Animal Health
Dedicated facilities in Haridwar for veterinary bolus, feed supplements, oral liquid drenches, and veterinary formulations.
Facility Audits & Regulatory
Schedule physical or virtual WHO-GMP facility audits across our Haridwar (Units I & II) and Aligarh (Unit III) plants, CTD dossier support, and COPP documentation.
Common Questions
Frequently Asked Questions
Quick answers regarding manufacturing contracts, minimum order quantities, and facility audits.
Where are Evaron's primary pharmaceutical manufacturing plants located?
Our manufacturing operations are established across three strategic hubs: Unit I in Industrial Area, Bahadrabad, Haridwar (Uttarakhand); Unit II in Village Khata Kheri, Near Dev Bhoomi Industrial Area, Puhana, Roorkee (Uttarakhand); and Unit III on Ramghat Road, Aligarh (Uttar Pradesh). All three plants adhere to rigorous WHO-GMP quality standards.
What is the typical lead time for third-party commercial production?
For existing approved formulations, standard commercial production cycles run between 3 to 4 weeks from raw material QC clearance. For new product registrations or custom formulations requiring artwork and stability data, the initial batch turnaround is typically 45 days.
What documents are required to initiate contract manufacturing?
To manufacture formulations under your brand name, standard regulatory documentation includes: (1) Copy of Drug License (Form 20B/21B), (2) GST Registration Certificate, (3) Trademark Registration / Brand Authorization Certificate, and (4) Non-Resemblance declaration.
How do we schedule a physical plant audit at Haridwar, Roorkee, or Aligarh?
Plant visits and technical quality audits across our three manufacturing units (Unit I, Unit II, or Unit III) can be scheduled by contacting our Quality Assurance team at least 5 business days in advance. Call our team directly at +91-8006005699 or email contact@evaronpharmaceutical.co to arrange visit clearance.
Partner With Evaron Pharmaceuticals
Speak with our technical manufacturing specialists across Haridwar (Units I & II) & Aligarh (Unit III) to explore formulation contracts, batch scales, or product dossiers.