ACPL

Best Pharmacovigilance Services Provider in Noida End-to-End Drug Safety and Compliance Solutions We at ACPL provide exhaustive Pharmacovigilance (PV) services aimed at assisting pharmaceutical, biotechnology, and medical device organizations with worldwide safety and regulatory demands. With 25+ years of rich experience and a team of specialized professionals, we guarantee complete…

Materiovigilance Services in India – Stay Compliant with ACPL In a country like India where the healthcare sector is rapidly evolving, ensuring the safety and performance of medical devices is of utmost importance. This is where Materiovigilance plays a critical role. At Accredited Consultants Pvt. Ltd. (ACPL), we provide expert…

Simplifying Compliance Certifications in Noida – Partner with ACPL In today’s rapidly evolving regulatory environment, compliance is not just a necessity – it’s the backbone of business credibility. At Accredited Consultants Pvt. Ltd. (ACPL), based in Noida, we take pride in being a one-stop solution for all your compliance certification…

Simplifying Compliance Certifications in Noida – Partner with ACPL In today’s rapidly evolving regulatory environment, compliance is not just a necessity – it’s the backbone of business credibility. At Accredited Consultants Pvt. Ltd. (ACPL), based in Noida, we take pride in being a one-stop solution for all your compliance certification…

New MoCRA Adverse Event Reporting Requirements: Impact on the Cosmetic Industry Product safety and consumer protection are the cornerstones of the cosmetics industry, now reinforced by regulatory milestones like the Modernization of Cosmetics Regulation Act (MoCRA) of 2022 and its 2023 amendment. These legislative advancements underscore the rising importance of…

India may soon start training drug regulators from select foreign countries on drug regulatory practices and pharmacovigilance, officials familiar with the matter said on Wednesday. The project could involve drug regulators and inspectors from African, Southeast Asian, and South Asian Association for Regional Cooperation (SAARC) countries, focusing on drug regulatory…

Regarding manufacturers requesting an extension to adopt the updated Schedule M, the Central Drugs Standard Control Organization (CDSCO) has developed an online application process via the Online National Drugs Licensing System (ONDLS) (www.statedrugs.gov.in). Manufacturers seeking an extension to adopt the updated Schedule M can apply online through the Online National…

Pharmacovigilance in African Countries: Progress and Initiatives African nations have made significant strides in strengthening pharmacovigilance systems to ensure medicine safety and protect public health. Through collaborative efforts and regulatory harmonization, these countries are developing robust mechanisms for monitoring adverse drug reactions (ADRs) and ensuring safer healthcare outcomes. 1. DNDi…