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Whether you need a new website, brand video or social media campaign, SCORR can deliver. Our services include web design, development & hosting; video/animation; SEO/SEM; marketing automation & CRM management; and performance metrics.

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We provide regulatory services with a track record of supporting regulatory approvals for oral dosage forms in US, Europe, etc. We ensure registration & post-approval strategies, regulatory agency inquiries & inspections and lifecycle management support

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ChemWerth has access to over 500 APIs from more than 30 manufacturing facilities in the U.S., Europe, India and China. cGMP compliant facilities for Antibiotics, Inorganic Compounds, Organometalic Compounds, Polypeptides, Complex Organic Compounds.

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Our Regulatory team provides compliance & regulatory support by managing documentation creation, review and submission while our Compliance group manages our Factory Compliance Programs, CMO management and facility inspections.

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Beyond the preparation of regulatory documentation, Medichem is ready to support the customer from the registration of the Marketing Authorizations to their approval in order to reach the market as quick as possible.

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Bachem also has a strong regulatory background and we are well prepared to fully support you with the required regulatory documentation such as drug master files (DMFs)

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Pharma Business Unit has an extensive portfolio of products including various active ingredients in various therapeutic categories, as well as excipients and natural plant extracts for solid formulations, semi-solid, liquid and injectable.

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Inabata France implemented the Good Distribution Practices (GDP) for distribution of APIs, Intermediates & Chemicals etc.

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Inabata France implemented the Good Distribution Practices (GDP) for distribution of APIs, Intermediates & Chemicals etc.

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We offer scientific and regulatory services for the pharmaceutical industry and our suppliers (APIs and finished drugs, human and veterinary), primarily in the areas GMP, audits and inspections as well as regulatory affairs (eCTD).

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Ningbo Transo-Pharm is active in API, qualifies manufacturers for full compliance, making it a valuable sourcing agent for clients and regulatory marketing agent for API manufacturers.

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Transo-Pharm, active in API, qualifies manufacturers for full compliance, making it a valuable sourcing agent for clients and regulatory marketing agent for API manufacturers.

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Transo-Pharm, active in API, qualifies manufacturers for full compliance, making it a valuable sourcing agent for clients and regulatory marketing agent for API manufacturers.

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Transo-Pharm, active in API, qualifies manufacturers for full compliance, making it a valuable sourcing agent for clients and regulatory marketing agent for API manufacturers.

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Rochem’s Regulatory group ensures that all Pharmaceutical, Nutritional, and Food products meet their applicable monograph/standard (USP/NF/EP/FCC) and are always labeled and packaged correctly.

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Wavelength offers complete regulatory support to its customers throughout the product life cycle, starting from early development, through filing and commercial sales, to assure market leadership and sustainability.

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Gentec Pharmaceutical Group offers documentation of the registristration dossier and follow up of its evaluation.

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Combining process chemistry expertise with analytical solutions for your program, Eurofins CDMO provides API development services and commercialization support from route scouting through to commercialization.