ISO 15378 Certification is a quality assurance for primary packaging materials for medical products specific prerequisites the USA for the utilization of ISO 9001:2008, with reference to GMP. Having a certificate of ISo15378 means you have managed different types of risk related to contamination, fault, and mistakes.  Operon strategist leading medical device regulatory consultant assist manufacturers to get ISO 15378 certification easily. 

In 2006, the procedure-oriented ISO 15378 standard was delivered. In view of the globally acknowledged ISO 9001 quality standard, it contains all the GMP essentials appropriate to primary packaging material, for example, batch tracing, risk management, validation, and controlled environment. 

What is ISO 15378 QMS Certification? 

  • ISO 15378:2017 standard indicates requirements for a quality management system where an organization needs to show its capacity to give primary packaging materials for medicinal products, which reliably meet customer requirements, including regulatory requirements and International Standards relevant to primary packaging medicinal materials 
  • An ISO 15378:2017 certificate with its wholistic way to deal with GMP and quality necessities is perceived all through the world. It delivers manufacturers of primary packaging materials with an appropriate capability for customer approval – just as improving the organization’s image according to the authorities. ISO 15378:2017 applies to all manufacturers of packaging materials that come into direct contact with medical products. The standard covers all the typical materials, such as glass, rubber, aluminum, and plastics. 
  • This ISO standard is currently lined up with ISO 9001:2015 and has the same 10 elements high-level structure. ISO 15378:2017 determines necessities for a quality management system where an association needs to exhibit its capacity to deliver primary packaging materials for medicinal products, which reliably meet customer requirements, including regulatory prerequisites and International Standards pertinent to primary packaging materials. 
  • Objective to upgrade customer satisfaction through the effective use of the system, including processes for the development of the system and the confirmation of conformity to client and material statutory and regulatory necessities. 
  • The primary packaging material is identified as the material that is in direct contact with the measurement structure. With the involvement in Primary packaging standard which may require any single part of a container closure system which includes containers, container liners, closures, closure liners, stopper oversells, etc. 

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What are the benefits of ISO 15378 Benefits? 

  • ISO 15378 Standard has strategic tools that reduce costs by minimizing waste and manufacturing errors and increasing productivity. 
  • It encourages organizations to get to new markets and encourages free and reasonable worldwide exchange. 
  • The manufacturer of USA or anywhere in globe can improve their proficiency of production processes by following GMP standards according to ISO 15378 standard. 
  • To relieve your risks particularly identified with product contamination, mix-ups and errors and ensure product efficacy and shelf life. 
  • Assurance of quality products to your clients. Upgrade customer satisfaction. 
  • Competitive Advantage over other non- confirmed providers. 
  • Application of risk management helps to reduce errors associated with the product. 

Application of ISO 15378 

  • ISO 15378:2017 is an application standard for the structure, manufacture and supply of primary packaging material for medicinal products. 
  • It is additionally appropriate for certification purposes of primary packaging material for medicinal products in pharmaceuticals and medical device industries. This primary packaging standard discovers good manufacturing practice (GMP) standards and Quality Management System relevant to primary packaging materials for medicinal products. 
  • ISO 15378 can be utilized for quality improvement, training, auditing and certification. 
  • The ISO 15378 standard is assessed every 5 years. 

What will be the Role of Operon Strategist? 

Our team can perform various activities like GAP analysis, QMS implementation and others. After understanding the need of ISO 15378, by performing GAP analysis and QMS we can assist you in creation of documentation and training. We also provide medical device consultation for India, Saudi Arabia, USA, Costa Rica, Oman, South Africa & United Kingdom. For free consultation Contact us now.

How will Operon Strategist help you in ISO 15378? 

Operon Strategist helps manufacturers to develop quality management systems as per the requirements of ISO 15378. We assist with documentation, training & implementation of the quality system. We help the Primary packaging material manufacturers to understand the requirements of ISO 15378 by performing GAP analysis and implementing QMS and GMP requirements as per ISO 15378:2017. As medical device regulatory consulting company We support the manufacturers of primary packaging materials for the medicinal products to enhance their QMS system by addressing specific requirements to meet the quality objectives as per ISO 15378 certification.