Manufacturing

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Our state-of-the-art manufacturing facility complies with current Good Manufacturing Practices (cGMP) and is approved by national regulatory agencies. In addition to this, we have UKAS accreditation of ISO 9001:2015, ISO 14001:2015, ISO 22000 and working strategically and technically to acquire ISO 17025.

Quality underlies everything we do.

Genetics undertakes a thorough validation of all manufacturing process and safety review for its products before they are set out for patient use. This review includes many of the steps outlined in the FDA draft “Guidance for Industry, Best Practices in Developing Proprietary Names for Drugs.” We also undertake a thorough search and development of database of product names for look-alike or sound-alike similarity that might result in confusion that could lead to a medication or a manufacturing error.

Genetic Health Care is committed to:

• Comply with all national and international statutory and regulatory requirements related to its

             products and activities, and mutually agreed customer requirements related to Food Safety.

• Set food safety objectives and allocate appropriate resources to achieve these objectives.

• Execution of “Risk Base Thinking” to control any probable hazard in the product and achieving

             highest level of customer satisfaction.

• Selection of Competent Food Safety Team and empower every Team Member through

             professional and personal development to ensure implementation of ISO 22000:2018 (FSMS) in

             true means.

• Continually improve its food safety system performance, products, processes, infrastructure,

             environment for operations and human resources by implementing Plan, Do, Check, Act activity.

• Review this policy at defined intervals for continuing stability.

• Ensure that this policy is available, communicated and implemented at all levels within the

             organization and all stakeholders.

Genetics Pharmaceuticals (Pvt.) Limited is committed to:

1. Preventing quality and environmental problems by identifying, addressing, and

    managing risks and opportunities, including those that can affect conformity of

    pharmaceuticals & nutraceuticals products rather than detecting and correcting

    them after they occur.

2. To fulfill or exceed customer needs and expectations by delivering a quality

    products in a consistent and timely manner.

3. Achieve utmost customer satisfaction by ensuring safe and reliable products.

4. Empower team members through professional and personal development;

5. Foster a workplace culture where our principal concern is to guarantee the

    physical integrity of our employees.

6. Identify IMS objectives and training needs by continuous review and monitoring

    of its processes and activities.

7. Reduce and where possible eliminate waste and prevent pollution at source.

8. To ensure that protection of the environment is firmly embedded in both the

    company’s and all employees culture and will Endeavour to influence its

    suppliers and customers in a similar strategic environmental manner.

9. Empower all employees to actively report unsafe conditions and take actions to

    continually improve IMS culture.

10. Establish IMS audit system to monitor continual improvement for the

      development of IMS Culture.

11. Comply with all applicable quality and environmental legal and other regulations

      requirements.

12. Genetics shall follow principles of Health, Safety and Environment to ensure safety of its

      employees.

13. This policy is communicated to all employees, interested parties and displayed

      for information purposes. The policy is reviewed at defined intervals for

      continuing suitability.