Ecomplianceplus dedicated team of regulatory experts ensures that our product is updated from time to time as per latest guidelines, ensuring best practices for our clients. Ecomplianceplus regulatory suite provide a controlled process for creating, reviewing and publishing documents used for the initial submission to marketing authorization application and then after for product life cycle management which involves moving from manual process to system based process for better control, traceability and accountability of the dossier preparation tasks. Ecomplianceplus provides most flexible and scalable regulatory compliance suite for small startups to large enterprises achieving superior quality, in compliance with MHRA, EMA, FDA and other regulatory agencies.
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