GDPR Compliance update
April 18, 2018
We are in process of rolling out organization-wide update (internal and external) to comply with upcoming deadline of GDPR. Test Collab will be fully compliant with GDPR before the 25th May 2018 deadline.If you have any questions or suggestions regarding GDPR compliance, reach us out from 'Contact us' link below.
Certifications for medical devices startups
This blog provides an overview of the various certifications required for medical device startups to bring their products to market. It covers certifications such as ISO 13485, FDA 510(k), CE Marking, and Health Canada Medical Device Licence. The importance of early planning and a strong quality management system in ensuring regulatory compliance and speeding up the process of getting to market.
Enforcing AI ethical framework in your testing
Startups have a responsibility to ensure that their AI systems are designed and used in a way that aligns with ethical principles, such as fairness, transparency, and non-discrimination. Ethical AI practices help to build trust with stakeholders, including customers, partners, and regulators, who may be concerned about the impact of AI on society. Learn more on how to make progress towards responsible AI