At Nex Pharma, we are committed to ensuring the safety, quality, and appropriate use of all pharmaceutical and healthcare products we supply. Our policies adhere to the highest regulatory standards set by the Ministry of Health Malaysia (MOH) and are continuously reviewed by our Pharmaceutical Compliance Board.
Who We Supply
Nex Pharma operates as a B2B pharmaceutical and healthcare supplier, providing products to:
- Pharmacies (independent & chain pharmacies)
- Medical clinics and general practitioners (GPs)
- Hospitals and specialist healthcare providers
- Healthcare facilities, wellness centers, and medical wholesalers
Scope of Products Supplied by Nex Pharma
We provide a comprehensive range of healthcare products, categorized as follows:
1. Prescription & Pharmacy-Only Medications (Regulated by MOH)
- Group B: Prescription-Only Medicines (POM) – Supplied only to licensed doctors, clinics, hospitals, and pharmacies with valid regulatory credentials.
- Group C: Pharmacy-Only Medicines – Dispensed to pharmacies and clinics for regulated patient distribution.
- Over-the-Counter (OTC) Medications – Provided to pharmacies and healthcare retailers for general sale.
2. Supplements & Functional Nutrition
- Vitamins, minerals, and herbal supplements
- Medical nutrition (e.g., enteral nutrition, protein supplements)
- Probiotics and digestive health supplements
3. Medical Devices & Consumables
- Diagnostic devices (e.g., blood glucose monitors, blood pressure monitors)
- Surgical consumables, PPE, and wound care supplies
- General medical consumables for clinical use
4. Personal Care & Wellness
- Skincare and hygiene products
- Pain relief and muscle recovery solutions
- General healthcare and wellness consumables
Regulatory Compliance & Verification
Nex Pharma ensures all pharmaceutical and medical supplies adhere to:
- Malaysian Poisons Act 1952
- Medical Device Act 2012
- National Pharmaceutical Regulatory Agency (NPRA) guidelines
- Good Dispensing Practice (2016)
All healthcare providers and institutions we supply must provide valid licensing and comply with MOH regulations.
Prescription Drug Dispensation & Supply Policy
1. Prescription Medications Supply (POM & Group C)
- Only supplied to licensed pharmacies, clinics, and hospitals with MOH-approved licenses.
- Prescription orders require proof of a valid Poison A/B License before fulfillment.
- Specialist-only medications require additional verification.
2. Partner Pharmacy & Clinic Approval Process
- Pharmacies & Clinics must comply with Malaysian Poisons Act 1952 regulations for dispensing medications.
- Pharmacists and doctors are responsible for final verification before patient dispensation.
- Nex Pharma reserves the right to reject orders if misuse or non-compliance is suspected.
3. Restricted & High-Risk Medications
- Nex Pharma does not supply medications requiring frequent monitoring or those with high misuse/addiction potential.
- Cold-chain products (e.g., insulin, vaccines) are available only to hospitals and licensed facilities with cold-chain logistics compliance.
- Unregistered or banned products in Malaysia are not supplied.
Ordering & Compliance for Healthcare Providers
1. Licensing & Account Verification
To purchase from Nex Pharma, all pharmacies, clinics, and medical institutions must provide:
- Valid Poison A/B License (for pharmaceutical orders)
- Medical Device Authority (MDA) registration (for medical devices)
- Company registration and MOH approvals
2. Bulk Ordering & Delivery
- Bulk supply is available for hospitals, clinics, and pharmacies.
- Orders undergo multi-level verification before dispatch.
- Logistics partners comply with MOH storage and transportation standards.
Pharmaceutical Compliance Board & Governance
Nex Pharma’s Pharmaceutical Compliance Board—comprising medical and pharmaceutical experts—ensures ongoing policy review and regulatory alignment. Our governance framework focuses on safety, quality assurance, and compliance with MOH and NPRA regulations.
Regulatory References
- Ministry of Health Malaysia (MOH) – Poisons Act 1952 & Medical Device Act 2012
- NPRA – Drug Registration Guidance Document (2016)
- Good Dispensing Practice (2016)
- Framework for Good Governance (2009)
- Malaysia, P. B. – Code of Conduct for Pharmacists and Bodies Corporate (2009)
- Poisons Regulation 1989
- Medical Device Authority Malaysia Guidelines
