ISO 20737
ISO 20737:2021 sets forth standardized guidelines to enhance transparency, reproducibility, and replicability in scientific research within health and social science disciplines. It supports ethical research practices and promotes the open dissemination of study protocols, datasets, and findings to reinforce public trust in science and policy-making.
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What is ISO 20737?
ISO 20737:2021 titled “Health informatics — Transparency and reproducibility — Guidance for documentation and data sharing” outlines requirements for making research data more accessible and verifiable. This standard is vital for research institutions, academic publishers, healthcare policy agencies, and organizations that conduct or sponsor studies.
Why is ISO 20737 important?
With increasing concerns about data manipulation and unverified claims in published research, ISO 20737 offers a structured way to ensure study reproducibility and public access to methodologies. It empowers stakeholders—including researchers, funders, and end-users—to assess the credibility of scientific outcomes, which is especially important in health and social policy decisions.
What are the benefits of ISO 20737?
- Encourages ethical and transparent research practices
- Promotes open-access policies and responsible data sharing
- Supports replicable study designs across multiple scientific disciplines
- Enhances peer review efficiency through standardized reporting
- Builds a foundation of trust in evidence-based policy-making
- Assists funding agencies in monitoring the quality and impact of supported research
What kind of businesses can benefit from ISO 20737?
✅ Improved Research Integrity: Organizations gain credibility by adhering to globally accepted transparency standards.
✅ Better Policy Decisions: Supports decision-making based on verified and reproducible data.
✅ Global Collaboration: Enhances cooperation between international research bodies through standardized data practices.
✅ Academic Recognition: Facilitates publication in reputed journals that prioritize transparent research.
✅ Compliance Assurance: Demonstrates commitment to ethical research, helping with audits and grant validations.
Top Tips on making ISO 9001 effective for you.
#1
Top management commitment while practicing and accomplishing the standard is the key to success.
#2
Keeping staff informed about the ongoing practices, a well-communicated plan would increase the motivation and zeal of working in them.
#3
Making sure that the various departments of the organization work as a team for the benefit of the organization and customers as well.
#4
Review systems, policies, processes, and procedures for a smooth working of QMS.
#5
Speaking to customers & suppliers while getting feedback & working on improvements.
#6
Training staff carrying out the internal audits with the opportunity for improvement.
#7
Celebrate your achievement and use the QualityAsia Assurance Mark on your literature, promotional material, and website.
#8
Ensure continuous improvement by regularly reviewing and updating your quality management practices.
#9
Promote a culture of quality by encouraging innovation, accountability, and employee involvement at every level of the organization.
Why QualityAsia?
QualityAsia always vanguard in the auditing and governing of internationally acclaimed standards practices. At QualityAsia, we focus on driving the success of our clients through creating excellence with our trained professional auditors. The content of our service provision, comply with international certification rules defined by the accreditation bodies without burning a hole in your pocket. We will take you through the journey of audits with our best kept audit practices, viz.:
Initial Certification – Stage 1 (Preparatory Phase)
- Thorough documented information review.
- Exchange of information with staff through online or onsite presence.
- Identification of key performances, processes & objectives as per the standard requisites.
- Analysis of facilities, infrastructure, systems and processes in regard with the requested certification scope with a resource allocation review.
Initial Certification – Stage 2 (On-site Audit)
- Measurement, reporting & reviewing the performances against key performances objectives.
- Reviewing the suitability of the system meeting the legal, regulatory & contractual requirements.
- Operational control of processes, internal audits & management reviews while understanding the responsibilities for the policies.
- Conclusion based on prescriptive requirements, policy, performance objectives, staff skill, operations, procedures, internal audits, etc.
Surveillance & Certification Renewal
Drawing out the scrutiny on various aspects of the previously done audits on effectiveness while reviewing the various processes and control of the operations in the QMS and finally going for the recertification.
