Post Buy Requirement
dsj Management Systems Solutions
Pune, Maharashtra, India
gstGST : 27BPWPJ9079J1ZS Verified Add Review

Certification Services #7199584

Integrated Management System Certification

An integrated management system (ims) integrates all organizations systems & processes, combine all related components of a business into one system for easier management and operations organization to work as a single unit with unified objectives. Quality, environmental and safety management systems are often combined and managed as an ims. Organizations often focus on management systems individually, often in silos and sometimes even in conflict. A quality team is concerned with the qms, often an ehs manager handles both environmental and health and safety issues, or a qhse manager handles safety, health, environment and quality, etc. The three management systems share many common requirements and the continual improvement goal. They differ in their approach and degree of prescription, but the ISO 9001, ISO 14001 and ISO 45001 standards are compatible in content, terminology & many of the requirements. It is often more efficient to combine the three systems (QMS, EMS & OHSMS) into one and sharing the common clauses and procedures. Benefits of integrated management system> consistent objectives, planning, and document management> implementation and operation of the system cost less.> Easier internal audits> no redundancies, reducing the chance of conflict.> Cost reduction due to integrated audits and assessments, as well as optimize processes and resources.> Optimize processes and resource
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CE Marking Certification Services

We see capital letters CE on many products in free movement in the European Economic Area. This marking, meaning Conformity with Europe, demonstrate that the products have been audited/assessed in terms of minimum safety, health and environmental requirements.You would see CE marking on a new telephone, food processor, TV set or crayons purchased in the European Community. CE marking also indicates fair competition among manufacturers as it enforces accountability and conformity with the same requirements. CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in the EEA. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area. CE marking is described as a trade passport because it enables the free movement of products within the European market. According to EU legislation, the EU Member States are not allowed to restrict the placing on the market of CE marked products, unless such measures can be justified on the basis of evidence of the non-compliance of the product. CE marking does not indicate that a product was made in the European Union. The CE mark also is not a quality mark. The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives.
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GMP Certification

Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects. GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made. WHO has established detailed guidelines for good manufacturing practices? Many countries have formulated their own requirements for GMP based on WHO GMP.
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  • Sourabh Jyotik (dsj Management Systems Solutions)
  • Pune-Satara Road, Dhankawadi, Pune-411043, Maharashtra, India,, Dhawadwadi
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  • Call 08069182237 Ext. 463
Service Provider of Certification Services from Pune, Maharashtra by dsj Management Systems Solutions
Post Buy Requirement
dsj Management Systems Solutions
Pune, Maharashtra, India
gstGST : 27BPWPJ9079J1ZS Verified Add Review

Certification Services #7199584

Integrated Management System Certification

An integrated management system (ims) integrates all organizations systems & processes, combine all related components of a business into one system for easier management and operations organization to work as a single unit with unified objectives. Quality, environmental and safety management systems are often combined and managed as an ims. Organizations often focus on management systems individually, often in silos and sometimes even in conflict. A quality team is concerned with the qms, often an ehs manager handles both environmental and health and safety issues, or a qhse manager handles safety, health, environment and quality, etc. The three management systems share many common requirements and the continual improvement goal. They differ in their approach and degree of prescription, but the ISO 9001, ISO 14001 and ISO 45001 standards are compatible in content, terminology & many of the requirements. It is often more efficient to combine the three systems (QMS, EMS & OHSMS) into one and sharing the common clauses and procedures. Benefits of integrated management system> consistent objectives, planning, and document management> implementation and operation of the system cost less.> Easier internal audits> no redundancies, reducing the chance of conflict.> Cost reduction due to integrated audits and assessments, as well as optimize processes and resources.> Optimize processes and resource
View Complete Details

CE Marking Certification Services

We see capital letters CE on many products in free movement in the European Economic Area. This marking, meaning Conformity with Europe, demonstrate that the products have been audited/assessed in terms of minimum safety, health and environmental requirements.You would see CE marking on a new telephone, food processor, TV set or crayons purchased in the European Community. CE marking also indicates fair competition among manufacturers as it enforces accountability and conformity with the same requirements. CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in the EEA. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area. CE marking is described as a trade passport because it enables the free movement of products within the European market. According to EU legislation, the EU Member States are not allowed to restrict the placing on the market of CE marked products, unless such measures can be justified on the basis of evidence of the non-compliance of the product. CE marking does not indicate that a product was made in the European Union. The CE mark also is not a quality mark. The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives.
View Complete Details

GMP Certification

Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects. GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made. WHO has established detailed guidelines for good manufacturing practices? Many countries have formulated their own requirements for GMP based on WHO GMP.
View Complete Details
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