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Home All Services (26) PS 9000 certification in Delhi ...
PS 9000 adopts a risk assessment approach to the identification and implementation of preventive action and uses case studies to illustrate areas of GMP risk.

PS 9000 is a standard relevant to all parts of the pharmaceutical industry supply chain, allowing shared knowledge, practices and implementation to manage risks and safeguard the well being of people and business.

Whether a contractual need or simply looking to reduce overall risk to your organisation and products, there are a number of key benefits to implementing a certificated PS 9000 system.

Quality Controls - Clear implementation of practices across production process including electronic interfaces to assure quality products, fit for purpose and minimising counterfeit medicines

Personnel/Communication - More clearly understand roles and responsibilities in terms of producing quality products

GMP - Incorporation of specific Good Manufacturing Practice requirements which assure material are appropriate quality and correct procedures are followed in terms of checking, traceability, contamination and hygiene controls

Risks - Structured approach to risk management and key focus on risk areas associated with packaging operations, with effective controls and activities detailed, which ultimately helps to reduce potential product and business issues

Compliance - Used in support of regulatory compliance and identification of appropriate legislation

Harmonisation - Helps integration of Regulatory, Quality and GMP requirements

Commitment - Organisations need to show their compliance with all relevant statutory and regulatory pharmaceutical packaging safety and GMP requirements in addition to their own policies.

PS 9000 certification in Delhi, Haridwar, Kashipur, India for Pharmaceutical Packaging company

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PS 9000 adopts a risk assessment approach to the identification and implementation of preventive action and uses case studies to illustrate areas of GMP risk. PS 9000 is a standard relevant to all parts of the pharmaceutical industry supply chain, allowing shared knowledge, practices and implementation to manage risks and safeguard the well being of people and business. Whether a contractual need or simply looking to reduce overall risk to your organisation and products, there are a number of key benefits to implementing a certificated PS 9000 system. Quality Controls - Clear implementation of practices across production process including electronic interfaces to assure quality products, fit for purpose and minimising counterfeit medicines Personnel/Communication - More clearly understand roles and responsibilities in terms of producing quality products GMP - Incorporation of specific Good Manufacturing Practice requirements which assure material are appropriate quality and correct procedures are followed in terms of checking, traceability, contamination and hygiene controls Risks - Structured approach to risk management and key focus on risk areas associated with packaging operations, with effective controls and activities detailed, which ultimately helps to reduce potential product and business issues Compliance - Used in support of regulatory compliance and identification of appropriate legislation Harmonisation - Helps integration of Regulatory, Quality and GMP requirements Commitment - Organisations need to show their compliance with all relevant statutory and regulatory pharmaceutical packaging safety and GMP requirements in addition to their own policies.
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  • 2017-11-18T07:33:25
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