This HMG API is designed for pharmaceutical manufacturers, formulation development teams, and quality control laboratories requiring consistent, documented gonadotropic activity for injectable and related dosage form development.

Each production batch undergoes rigorous testing for potency, purity, and biological activity, with complete analytical documentation supporting GMP-aligned workflows and regulatory submissions.

What is Human Menopausal Gonadotrophin (HMG)?

Human Menopausal Gonadotrophin (HMG) is a highly purified gonadotropic hormone preparation containing both Follicle-Stimulating Hormone (FSH) and Luteinizing Hormone (LH). It is supplied as a pharmaceutical-grade API for fertility and reproductive health formulations.

Key Specifications & Technical Details

Documentation Provided

• ▸ Certificate of Analysis (COA)
• ▸ MSDS / TDS
• ▸ Activity assay reports
• ▸ Sterility or endotoxin data (on request)

Applications of HMG API

Handling & Reconstitution Guidance

• ▸ Reconstitute with sterile water or physiological buffer
• ▸ Handle under aseptic conditions
• ▸ Avoid extreme pH or oxidizing agents
• ▸ Maintain full batch traceability
• ▸ Use promptly or store per validated protocols

Supplier & Procurement Process

• Sample Evaluation: Activity, solubility, assay compatibility
• Documentation Review: COA, TDS, analytical data
• Scale-Up: Bulk supply under agreed lead times and formats

Frequently Asked Questions

Q. Can I order samples?

Yes, small quantities are available for validation.

Q. Is custom packaging available?

OEM and custom labeling can be arranged.

Q. How fast is bulk supply?

Lead times are confirmed after sample approval.

Summary

HMG API is a well-documented, pharmaceutical-grade gonadotropin raw material supporting reproductive therapy development from early R&D to commercial manufacturing.