Regulatory

Regulatory compliance, supported by documented processes.

Learn more about the regulatory framework applicable to our activities. Relevant regulatory documentation is available to verified customers and partners upon request.

Regulatory framework

Key regulatory areas

Wholesale distribution

The wholesale distribution of medicinal products is carried out in accordance with applicable legal, regulatory and licensing requirements.

Good Distribution Practice (GDP)

Good Distribution Practice (GDP) requirements are designed to protect the quality and integrity of medicinal products throughout the distribution chain.

Quality complaints & pharmacovigilance

Quality and safety-related reports are handled in accordance with applicable procedures and responsibilities.

Recalls & withdrawals

Defined procedures are in place to support the timely management of product recalls, withdrawals and related communications.

Falsified medicinal products

Measures to help prevent falsified medicinal products from entering the legal supply chain form part of the applicable safety framework.

Data protection

Personal data are processed in accordance with applicable data protection legislation and internal procedures.

Need documentation?

Verified customers and partners can request relevant documentation or access documents made available through the Client & Partner Portal.

Our facilities and operations

HM Pharma
HM Pharma
HM Pharma

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