1. Home

제조 규정 준수

제조 규정 준수는 기술적, 법적 및 기업적 요구사항을 통합하고 제품 생산 및 마케팅을 목표로 하는 동시에 위험을 완화하고 소비자 안전을 보장하며 품질 표준을 충족하는 규정 준수를 보장합니다.

What is manufacturing compliance?

규정 미준수의 위험은 최근 몇 년 동안 특히 여러 국가 및 관할권에서 운영되는 제조업체의 경우 갈수록 더 중요한 문제가 되고 있습니다. 특정 산업 부문에서 정부 규제 기관의 역할이 증가하고 점점 더 글로벌화되는 제조업의 특성을 해결하기 위한 글로벌 제조 규정 준수 표준이 등장함에 따라 증가하는 제조 규정을 충족하기가 더 어려워지고 있습니다.

이처럼 늘어나는 제조 규정을 준수하기 위해 현재 많은 기업이 QMS(품질 관리 소프트웨어) 솔루션의 필수 구성 요소를 나타내는 규정 준수 소프트웨어 및 문서 관리 소프트웨어를 사용하고 있습니다.

제조업체가 세계화가 증가하고 제품 개발 비용이 증가하는 환경에서 경쟁력 있는 제품을 생산하고, 수익성 있게 운영하고, 비즈니스를 성장시킨다는 전략적 목표를 추구할 때 제조 규정 준수를 고려해야 합니다. 의료기기 및 생명 공학 제조에서 자동차 산업에 이르기까지 다양한 시장 부문에서 이러한 목표를 달성하기 위한 노력은 동일한 국가 내에서도 다양한 규제 기관에서 제조 규정 준수를 요구하고 있으므로 훨씬 더 어렵습니다. 예를 들어, 미국의 제조업체는 FDA(미국 식품의약국), EPA(환경 보호국), OSHA(직업안전위생국) 및 SEC(증권거래위원회)의 품질 표준 및 규정을 준수해야 합니다.

다음과 같은 여러 영역에 대한 제조 규정 준수는 제조업체에 직간접적으로 영향을 미칠 수 있습니다.

  • 제품 안전
  • 건강, 안전 및 환경 영향
  • 데이터 보호
  • 수출 통제
  • 부패 방지
  • IT 안전 및 보안
  • 공정한 경쟁
  • 고용법

관련 제품: Opcenter Quality, Teamcenter Quality and Compliance Management, Opcenter Execution

manufacturing-compliance-glossary

Understand the benefits

Consumer safety and product quality assurance

Adherence to regulations like Good Manufacturing Practices (GMP) ensures the implementation of robust quality systems and processes, minimizing risks associated with substandard products.

Operational eficiency and cost reduction

Streamline and optimize internal processes to meet industry and regulatory requirements, leading to improved productivity, reduced errors and proactive mitigation of potential disruptions.

Risk mitigation and legal protection

Identify and address potential regulatory issues, establishing a documented framework that demonstrates proactive adherence to standards and reducing the likelihood of legal issues or fines.

Types of manufacturing regulations and compliance mandates

Manufacturing compliance in some sectors – most notably, medical device and drug manufacturing – centers around the FDA’s manufacturing regulations. The core mandate guiding FDA regulatory oversight is consumer safety. As a result, the FDA has defined Good Manufacturing Practices (GMP) for both device and drug manufacturers, which dictate the measures that must be taken to ensure that quality systems and processes are in place to consistently produce safe, quality products. Therefore, manufacturers in these sectors seek a manufacturing certificate of compliance indicating that they meet GMP.

Software developers have responded to this need by creating solutions for managing regulatory compliance within QMS and manufacturing execution systems (MES). For those in manufacturing sectors regulated by the FDA, these solutions must be compliant with Title 21 CFR Part 11 and Part 820. Part 11 requires pharmaceutical manufacturers, medical device manufacturers, biotech companies, biologics developers, contract research organizations and other FDA-regulated industries (with some specific exceptions) to implement controls. These controls include audits, system validations, audit trails, electronic signatures, and documentation for software and systems involved in processing electronic data that are (a) required to be maintained by the FDA predicate rules or (b) used to demonstrate compliance to a predicate rule.

With the advent of globalization, international standards have become increasingly important to manufacturers looking to be compliant across international markets. With the implementation of the EMC Directive (i.e., European Machinery Directive) and similar regulations in other countries, regulatory compliance has become a major milestone in product development and marketing for most manufacturers. Key international industry standards for manufacturing compliance include:

  • ISO 9001
  • ISO 13485
  • IEC 61215
  • IEC 61646

Moreover, new and harmonized standards for manufacturing compliance continue to be developed.

Management Imperative for Compliance

Meeting the challenge of manufacturing regulatory compliance requires establishing a consistent top-down strategy for ensuring compliance across the enterprise.

If management fails to create an environment that ensures manufacturing compliance – or lacks documentation to prove all necessary steps have been taken to achieve it – it can be held accountable for compliance breaches. Because of this, manufacturing compliance must be an ingrained part of day-to-day business operations and therefore part of the organizational culture. Employee involvement in and acceptance of compliance tasks, including a complete understanding of manufacturing regulations, requirements and objectives, are integral parts of a sound compliance practice for manufacturing.

관련 제품

자세히 알아보기

eBook

Siemens Opcenter Quality 소프트웨어를 통해 제조업체의 품질 목표 달성

백서

모범 사례를 사용하여 품질 및 규제 준수 간소화