Makrocare
Member
MakroCare offers comprehensive Global Regulatory Publishing and eCTD Submission Services tailored to meet the diverse needs of pharmaceutical, biotechnology, and medical device companies worldwide. With the ever-evolving regulatory landscape and expanding global markets, our expert team
ensures seamless preparation, publishing, and submission of regulatory documents in compliance with international standards.
Drawing upon our deep understanding of regulatory guidelines and extensive experience across various regulatory authorities such as the FDA, EMA, PMDA, and others, MakroCare delivers efficient and accurate publishing solutions. Our services encompass document formatting, compilation, and publishing for electronic Common Technical Document (eCTD) submissions, ensuring consistency, quality, and adherence to regulatory specifications.
for more info: https://www.makrocare.com/biopharma/regulatory/operations/publishing/
ensures seamless preparation, publishing, and submission of regulatory documents in compliance with international standards.
Drawing upon our deep understanding of regulatory guidelines and extensive experience across various regulatory authorities such as the FDA, EMA, PMDA, and others, MakroCare delivers efficient and accurate publishing solutions. Our services encompass document formatting, compilation, and publishing for electronic Common Technical Document (eCTD) submissions, ensuring consistency, quality, and adherence to regulatory specifications.
for more info: https://www.makrocare.com/biopharma/regulatory/operations/publishing/
