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A Privacy Impact Assessment (PIA) Philippines collects and processes personal data from its customers. Companies should have a clear understanding of how the data flows through their system. Identifying privacy risks early and putting actions in place to address them ensures that companies comply with the Data Privacy Act of 2012 (RA 10173) and other data […]

In 2026, cyber threats are on the increase, and the global cybercrime is estimated to be between 1.2 trillion and 1.5 trillion annually. American corporations are losing their money in cybercrime to the tune of $639.2 billion, which predetermines a high demand among offensive security companies. It is reported that 131 new vulnerabilities are reported […]

India is expanding its digital health services by Ayushman Bharat Digital Mission. Researchers estimate the cybersecurity market in the country to grow to a minimum of 5.56 billion by 2025 and 12.9 billion by 2030, or an annual growth of 18.33% per year. The best safety badge is the ABHA Web Application security certificate. You […]

Innovative technology is not all one needs to enter the U.S. medical device market in 2026. It would require stiff regulatory alignment with the U.S. Food and Drug Administration. In the case of non-U.S. manufacturers, a stable FDA US Agent cannot be appointed as an option. It is a compulsory compliance provision and an important […]

The United States has one of the most regulated markets in medical devices, pharmaceuticals, and healthcare products. Interacting with the regulations of the United States Food and Drug Administration is an inevitable process that involves prudent planning and regulatory skills for Indian manufacturers planning to enter the US market. FDA regulations are organized, documented and […]

Modern medical devices are becoming more connected, software-driven, and dependent on digital technologies. This has extended the scope of regulatory expectations from product safety to cybersecurity, software integrity, data privacy, and supply chain security. As a result, medical device compliance is crucial throughout the product lifecycle, from design and development to post-market monitoring. According to […]

An increasing volume of cyber risks is affecting the UK’s financial ecosystem, which severely affects financial institutions. As a regulatory body, the Financial Conduct Authority has set very stringent regulations with regard to Operational Resilience. In addition, FCA compliance will directly relate the Cybersecurity Maturity of all Firms to Regulatory Trust with FCA. Penetration testing […]

Introduction Medical equipment utilized in the US is becoming software-enabled, networked, and under constant upgrade throughout its life cycle. Infusion pumps and imaging systems are now used in complex networked hospital environments and cloud-connected environments. This has changed Medical Device Vulnerability Management programs into a patient safety and regulatory requirement, and not a security capability. […]

Did you also know that in 2024, the OT-targeted cyberattacks increased by more than 150%? Manufacturing security audit programs are now crucial for securing industrial operations. In addition, the mean breach expenses have increased to over $25 million in manufacturing plants. Thus, the use of all-inclusive security is no longer a choice. The modern day […]