Regulatory Pharma NetRegulatory Pharma Net, regulatory affairs pharma.#Regulatory #affairs #pharma

Posted On Jun 12 2018 by

regulatory affairs pharma OUR GOAL IS TO EXCEED YOUR EXPECTATIONS OUR SERVICES Regulatory Affairs, Drug Development, Pharmacovigilance, Medical Writing, Pricing Reimbursement, Market Access Global and Local Regulatory Affairs Strategic Advice and Due Diligence Pricing & Reimbursement and Market Access Pharmacovigilance eCTD and Regulatory Procedures Management Medical Devices Project Management Orphan Drug Applications Pharmaceutical, Preclinical and Clinical Development Clinical Trial Applications Quality Management and Auditing Scientific / Medical Writing Product Information and Readability Testing Life Cycle Management Training Biocides, Food Supplements and Cosmetics ABOUT US Partner of many pharmaceutical companies, managing hundreds of multi-task projects, on a worldwide-scale EVENTS Discover next …


10th Annual Pharmaceutical Regulatory Affairs Summit Asia 2017 – IBC Asia, an Informa business, regulatory affairs pharma.#Regulatory #affairs #pharma

Posted On Jun 12 2018 by

regulatory affairs pharma With a 9-year track record of successfully bringing to market the latest developments and insights from decision makers, the Pharma Regulatory Affairs Summit remains the only such conference in Asia. Part of the PharmaCon suite of events, the conference affords you the opportunity of getting hot of the press information and networking across various pharma industry segments. “Met regulatory affairs from various companies across Asia and exchanged information regarding issues we have faced in registering the product.” Astuti Kurniati, Associate Principal Regulatory Specialist, PT Dexa Medical Conference Highlights: Regional Government updates on initiatives, reducing backlogs, new guidelines …


Pharma regulatory, pharma regulatory.#Pharma #regulatory

Posted On May 18 2018 by

pharma regulatory Spark Pharma regulatory consultant is an India based Pharmaceutical Regulatory consultant, Located in Surat and Ahmedabad, Gujarat, India. Spark Pharma regulatory consultant is involved in a wide variety of regulatory consulting assignments which Regulated markets e.g. U.S.A, Europe, Canada, Australia etc. and Less regulated markets e.g. India, Asia Pacific, CIS, Middle- East, Africa etc. Spark Pharma Regulatory is managed by a industry trained regulatory professional having invaluable Pharma experience from Reputed pharmaceutical company. We assist our clients by guiding the product development in line with the country specific requirements, data generation, document compilation for submission to various Regulatory …


Regulatory – Safety, pharma regulatory.#Pharma #regulatory

Posted On May 18 2018 by

Regulatory Safety PEOPLE ON THE MOVE Former Pfizer, Sanofi and Acacia execs on the move 22-Nov-2017 By Flora Southey In a game of hiring Tetris, an Eli Lilly alumni is promoted at Astellas, and former Sanofi chairman is employed by Pertinax Pharma. London to Amsterdam in 16 months a ‘demanding challenge’ says EMA 21-Nov-2017 By Flora Southey European member states have selected Amsterdam as the post-Brexit home of the European Medicines Agency, following a secret ballot vote in Brussels yesterday. Pfizer demands return of drugs set for use in US lethal injections 21-Nov-2017 By Dan Stanton The Big Pharma firm …


10th Annual Pharmaceutical Regulatory Affairs Summit Asia 2017 – IBC Asia, an Informa business, pharma regulatory affairs.#Pharma #regulatory #affairs

Posted On May 15 2018 by

pharma regulatory affairs With a 9-year track record of successfully bringing to market the latest developments and insights from decision makers, the Pharma Regulatory Affairs Summit remains the only such conference in Asia. Part of the PharmaCon suite of events, the conference affords you the opportunity of getting hot of the press information and networking across various pharma industry segments. “Met regulatory affairs from various companies across Asia and exchanged information regarding issues we have faced in registering the product.” Astuti Kurniati, Associate Principal Regulatory Specialist, PT Dexa Medical Conference Highlights: Regional Government updates on initiatives, reducing backlogs, new guidelines …


Regulatory affairs regulatory consulting services Poland, pharmaceutical regulatory affairs.#Pharmaceutical #regulatory #affairs

Posted On Mar 13 2018 by

Pharmaceutical regulatory affairs services Poland and EU Regulatory affairs for medicinal products or medical devices is a complex process. Each country in Europe has its own specific requirements related to medicinal products, medical devices or food supplements. Knowledge of such county-specific regulations is crucial to get marketing authorization or to solve other regulatory problems smoothly and quickly. It helps also to foresee and prevent from potential problems by choosing the right solutions in advance not during the authorization process when all problems and clarifications result in huge delays. Our services help to avoid such dead ends which is of great …


Home Armor Pharma – Armor Pharma, pharma regulatory.#Pharma #regulatory

Posted On Mar 5 2018 by

QbD in pediatric formulations a new poster with EXCIPRESS GR150! We are pleased to announce that a new poster has been published by Barcelona University using EXCIPRESS [ ] 80 mesh : a new sieved lactose grade available! We are pleased to announce the launching of our sieved lactose : ARMOR PHARMA lactose monohydrate 80M [ ] Many occasions to meet ARMOR PHARMA in 2017! We will be present at many pharma global events local seminars, Join us in 2017! Purity as a performance indicator Beyond the regulatory requirements, purity is for us the best performance indicator. A network of …


European pharmaceutical regulatory affairs experts – Pharma-EU, s, pharma regulatory.#Pharma #regulatory

Posted On Mar 5 2018 by

Pharma-EU.com: Pharmaceutical Regulatory Solutions for the European Union Consultations with patients regarding the package information leaflets. Guaranteed acceptance across the EU for National, MRP, DCP and CPs. Previously tested PILs can be used to support other PILs to create readability testing exemptions. Readability Testing of Package Information Leaflets and Bridging for the Generic Industry – download (285 kB) European Regulatory Pharmaceutical Consulting Services We can reformat and submit your pharmaceutical’s dossier to any member state in eCTD or CTD format. Our regulatory managers have proven their experience in coordinating and completing European procedures. We can work on-site as well as …


10th Annual Pharmaceutical Regulatory Affairs Summit Asia 2017 – IBC Asia, an Informa business, pharma regulatory affairs.#Pharma #regulatory #affairs

Posted On Mar 4 2018 by

pharma regulatory affairs With a 9-year track record of successfully bringing to market the latest developments and insights from decision makers, the Pharma Regulatory Affairs Summit remains the only such conference in Asia. Part of the PharmaCon suite of events, the conference affords you the opportunity of getting hot of the press information and networking across various pharma industry segments. “Met regulatory affairs from various companies across Asia and exchanged information regarding issues we have faced in registering the product.” Astuti Kurniati, Associate Principal Regulatory Specialist, PT Dexa Medical Conference Highlights: Regional Government updates on initiatives, reducing backlogs, new guidelines …


Pharma regulatory affairs, pharma regulatory affairs.#Pharma #regulatory #affairs

Posted On Mar 4 2018 by

pharma regulatory affairs Spark Pharma regulatory consultant is an India based Pharmaceutical Regulatory consultant, Located in Surat and Ahmedabad, Gujarat, India. Spark Pharma regulatory consultant is involved in a wide variety of regulatory consulting assignments which Regulated markets e.g. U.S.A, Europe, Canada, Australia etc. and Less regulated markets e.g. India, Asia Pacific, CIS, Middle- East, Africa etc. Spark Pharma Regulatory is managed by a industry trained regulatory professional having invaluable Pharma experience from Reputed pharmaceutical company. We assist our clients by guiding the product development in line with the country specific requirements, data generation, document compilation for submission to various …