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Pharmaceutical Product Registration (NPRA)

assist you to interact with the National Pharmaceutical Regulatory Agency (NPRA)

 

GMP Consulting

A Good Manufacturing Practices (GMP) certification scheme provides independent verification by NPRA

 

Medical Device Product Registration

Medical device product registration in Malaysia is overseen by the Medical Device Authority

 

GDPMD Consulting

Good Distribution Practices for Medical Devices

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Pharmaceutical Product Registration (NPRA)

assist you to interact with the National Pharmaceutical Regulatory Agency (NPRA)

 

GMP Consulting

A Good Manufacturing Practices (GMP) certification scheme provides independent verification by NPRA

 

Medical Device Product Registration

Medical device product registration in Malaysia is overseen by the Medical Device Authority

 

GDPMD Consulting

Good Distribution Practices for Medical Devices

1
1

Clientele

Why Choose Kazami Group

About Kazami

Preferred Consultant in Malaysia

Specialized expertise with over 35 years of extensive practical experience to assist in developing management systems from initial concept to establishment & successful implementation.

Quality System Auditing Expertise

Kazami Group conducts quality management system audits and factory inspections consistent with most international regulations and standards.

Single Source Solution

Kazami Group offers consulting services for major medical & non-medical device markets according to national & international standards and regulations.

Regional And Local Proficiency

Our regional quality management system experts understand regional and local regulations and knowledge needs.

Kazami Group Understands The Requirements

Kazami Group is a local company (Malaysia) who understands the requirements of the local authority and the needs of various industries. We are able to provide quality consultancy services and meeting the demands from these industries at affordable rates.

• 35 Years Of Experience 

• 35 Years Of Experience 

Kazami Group Offered Services

GDPMD Consulting Programme

The aim of GDPMD is to ensure that companies dealing with medical devices have a quality distribution system in place.

ISO 13485 Consulting Programme

An internationally agreed standard that sets out the requirements for a quality management system specific to the medical devices industry.

ISO 9001 Consulting Programme

ISO 9001 sets out the criteria for a quality management system. It can be used by any organization of any size, of any industry, and field of activity.

Medical Device Product Registration (MDA)

Our in-house team of local, experienced regulatory affairs specialists provide unrivalled assistance to medical device manufacturers and distributors alike who benefit from accessing real, on-the-ground expertise.

Pharmaceutical Product Registration (NPRA)

We provide strategic consultancy and advisory on product registration and assist our clients to interact with the National Pharmaceutical Regulatory Agency, NPRA (formerly known as National Pharmaceutical Control Bureau).

GMP Consulting Programme

A GMP is an important enhancement to your food safety management system, which increases your customers’ confidence in your commitment to trading and producing safe, high-quality food.

Training

We provide various training courses ranging from ISO standards, GDPMD, GMP, internal audit and customized courses based on clients’ needs.

Medical Device Product Registration (MDA)

Kazami Group is a regulatory affairs and market access consultancy service provider that specializes in the registration, authorized representation & importation of medical devices.

Pharmaceutical Product Registration (NPRA)

Kazami Group provides strategic consultancy and advisory on product registration and assist our clients to interact with the National Pharmaceutical Regulatory Agency, NPRA (formerly known as National Pharmaceutical Control Bureau) for a wide range of product applications including pharmaceuticals, cosmetics, OTC, and complementary medicines.

Training