ISO 15378 Certification for Primary Packaging
Operon Strategist offers comprehensive consulting for ISO 15378 certification, ensuring compliance with the international standard for primary packaging materials for medicinal products. Our expertise helps you achieve certification, focusing on quality and regulatory requirements specific to the pharmaceutical packaging industry.
ISO 15378 Primary Packaging Material for Medicinal Products
ISO 15378 Certification is a quality assurance for primary packaging materials for medical products specific prerequisites in Costa Rica for the utilization of ISO 9001:2008, with reference to GMP. 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 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 the 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 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.
Key Requirements of the ISO 15378 Standard
To achieve ISO 15378 certification, companies must adhere to strict guidelines that include:
Good Manufacturing Practices (GMP): Implementing GMP to maintain consistent quality.
Risk Management: Identifying and mitigating risks in the manufacturing process.
Documentation Control: Proper documentation and record-keeping to support compliance.
Supplier Management: Ensuring that suppliers also comply with quality standards.
Our consulting services cover all these aspects, helping you meet the requirements of the ISO 15378 standard.
ISO Training Services for Certification Success
We offer a range of ISO training services to support companies in their certification journey. Our training solutions include:
ISO 15378 Training: Comprehensive training to help your team understand the requirements and implementation of ISO 15378.
ISO 13485 Certification Training: A detailed course to guide companies through the quality management system requirements for medical devices.
ISO 13485 Internal Auditor Course: Equip your team with the skills to perform internal audits and ensure compliance with ISO 13485.
Training is crucial to maintain standards and facilitate a smooth certification process.
What are the Benefits of ISO 15378?
- 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 encourage free and reasonable worldwide exchange.
- The manufacturer of Costa Rica or anywhere in the 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 the medicinal product.
- 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 at every 5 years.
What will be the Role of the Operon Strategist?
Our team will perform various activities like GAP analysis, QMS implementation, and others. After understanding the requirement of ISO 15378, by performing GAP analysis and QMS we can assist you in the creation of documentation and training.
How will Operon Strategist help you in ISO 15378 Certification?
Operon Strategist helps manufacturers 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 understand the requirements of ISO 15378 by performing GAP analysis and implementing QMS and GMP requirements as per ISO 15378:2017. As a medical device regulatory consulting company, We support the manufacturers of primary packaging materials for medicinal products to enhance their QMS system by addressing specific requirements to meet the quality objectives as per ISO 15378 certification. Operon Strategist assists the pharmaceutical and medical device industries of Costa Rica to assess their suppliers of primary packaging materials and increase overall product quality. We also provide medical device consultation for India, Saudi Arabia, the USA, the UK, South Africa, Oman, Iran & Egypt. Feel free to contact us.