Question 1

Is Solunex Healthcare a WHO-GMP certified pharmaceutical manufacturer?

Accepted Answer

Yes. Solunex Healthcare Private Limited operates a WHO-GMP certified formulation manufacturing facility in Changodar, Ahmedabad, Gujarat, India, with quality systems aligned to global Good Manufacturing Practices.

Question 2

Which dosage forms can Solunex Healthcare manufacture?

Accepted Answer

Solunex manufactures oral solids (tablets and capsules), oral liquids (syrups, suspensions and solutions) and external preparations including creams, ointments, gels, lotions and antiseptic solutions.

Question 3

Does Solunex offer third-party and contract manufacturing?

Accepted Answer

Yes. Solunex provides end-to-end third-party (contract) manufacturing covering formulation development, commercial production, packaging, quality assurance and regulatory documentation for pharmaceutical marketers, distributors and exporters.

Question 4

What is the manufacturing capacity of Solunex Healthcare?

Accepted Answer

The facility supports more than 500 million units per year across multiple dosage forms, including a high-speed capsule line capable of up to 1,00,000 capsules per hour.

Question 5

Does Solunex support exports and regulatory documentation?

Accepted Answer

Yes. The regulatory team prepares CTD and eCTD dossiers, Certificates of Analysis, stability data, technical data sheets, method validation and export documentation to support local and international supply.

Question 6

How can I request a manufacturing quote from Solunex?

Accepted Answer

Share your dosage form, target market, pack format and estimated annual volume through the contact form, on WhatsApp at +91 99250 04620, or by email at connect@solunexhealthcare.com. The team typically responds within 24 hours.