MakroCare is expert strategic development and commercialization global partner for pharmaceutical, biotechnology and medical device industries. Our experience, programs and processes bring a new dimension to development strategy, regulatory/risk planning & management, clinical research, medical/scientific support and emerging region expansion. MakroCare has operations and presence in US, UK, EU, and Asia. MakroCare is well positioned to meet the demands of the expanding product portfolio needs of our life sciences clients worldwide. We also understand the demands of an increasingly competitive market.
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Regulatory CMC Changes for Pharmaceutical Products
All the biopharmaceutical companies must follow respective nation’s laws or regulations in order to develop, manufacture and sale their pharmaceutical products. Read our Blog @ http://bit.ly/2GS0V1H
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MakroCare is recognized as “The Outstanding Consulting Firms 2019”
MakroCare has recognized as an outstanding consulting firm by Insights Success in the Outstanding Consulting Firms 2019 magazine.
MakroCare is a leading consulting firm with a focus on BioPharma and Medical Devices industries. It specializes in Advisory, Clinical/Medical, Regulatory Affairs, and Product Support areas. Its global experience, process accelerators, and proprietary technology bring a new dimension to client’s product development, life cycle management, and compliance areas. Read more @ https://www.makrocare.com/news-section/2391-the-outstanding-consulting-firms-2019
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Global Regulatory Labeling Services
Labeling & Artwork Management solutions for Pharma industry from local label alignment, label updates, artwork creation and artwork pack management. Know more @ https://www.makrocare.com/biopharma/regulatory/labeling
#regulatory labeling services#global labeling#regulatory labeling#structured product labeling#spllabeling#Labeling Services#Regulatory Affairs Labeling#pharma label consulting
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Global Regulatory CMC Services
MakroCare CMC services include authoring of annual reports, drug master files, dossier amendments and supplements,preparation, publication and submission of electronic common technical document (eCTD) applications for Pharma, Biotech, life sciences industry. Read more @ https://www.makrocare.com/regulatory/authoring/cmc
#CMC regulatory strategy#CMC Reglatory Services#CMC outsourcing#Common Technical Document#regulatory affairs cmc#cmc services
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