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Pauels Consulting -Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -Nonclinical Project Development - Drug Regulatory Affairs

Scientific Consulting, Medical Writing,. Based on broad in-house expertise and a strong network of external partners and academic experts, Pauels Consulting can assist your drug development projects from planning of early pharmacodynamic studies through the design and monitoring of pharmacokinetic and toxicological programmes, to the final compilation of MAA documents. Besides classical small molecule pharmaceuticals, Pauels Consulting focuses on biotechnology derived drugs.

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Pauels Consulting -Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -Nonclinical Project Development - Drug Regulatory Affairs | pauels-scientific.de Reviews

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Scientific Consulting, Medical Writing,. Based on broad in-house expertise and a strong network of external partners and academic experts, Pauels Consulting can assist your drug development projects from planning of early pharmacodynamic studies through the design and monitoring of pharmacokinetic and toxicological programmes, to the final compilation of MAA documents. Besides classical small molecule pharmaceuticals, Pauels Consulting focuses on biotechnology derived drugs.

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1 nonclinical

2 preclinical

3 toxicity

4 toxicology

5 pharmacodynamics

6 pharmacokinetics

7 immunotoxicity

8 CTD

9 IMPD

10 CTA

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pauels consulting,drug regulatory affairs,office steinfurt,alleestr 18,germany,info@pauels scientific de,services,wwwpauels scientific de,enter,scientific consulting,pauels consulting 2008,cell based therapies,and immunologicals

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Pauels Consulting -Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -Nonclinical Project Development - Drug Regulatory Affairs | pauels-scientific.de Reviews

https://pauels-scientific.de

Scientific Consulting, Medical Writing,. Based on broad in-house expertise and a strong network of external partners and academic experts, Pauels Consulting can assist your drug development projects from planning of early pharmacodynamic studies through the design and monitoring of pharmacokinetic and toxicological programmes, to the final compilation of MAA documents. Besides classical small molecule pharmaceuticals, Pauels Consulting focuses on biotechnology derived drugs.

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pauels-scientific.de

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Pauels Consulting -Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -Nonclinical Project Development - Drug Regulatory Affairs

http://www.pauels-scientific.de/scientific.html

Scientific Consulting, Medical Writing,. Ng appropriate non-clinical development programmes encompassing pharmacodynamics, pharmacokinetics, and toxicology,. Pauels Consulting can assist you. There are many non-clinical questions to be answered before a Marketing Authorization (or even a clinical trial) can be granted. To speed up the development process, the answers should ideally be available before the Regulators ask for. In preparing regulatory/scientific advice meetings with the relevant authorities,.

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Pauels Consulting - Nonclinical Consulting (Pharmacology,Pharmacokinetics, Toxicology) - Nonclinical Project Development - DrugRegulatory Affairs

http://www.pauels-scientific.de/disclaimer.html

Scientific Consulting, Medical Writing. The author reserves the right not to be responsible for the topicality, correctness, completeness or quality of the information provided. Liability claims regarding damage caused by the use of any information provided, including any kind of information which is incomplete or incorrect,will therefore be rejected. 2 Referrals and links. 5 Legal validity of this disclaimer.

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Pauels Consulting -Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -Nonclinical Project Development - Drug Regulatory Affairs

http://www.pauels-scientific.de/impressum.html

Scientific Consulting, Medical Writing,. Verantwortlich nach 6 TDG und 10 MDStV:. Drrernat.habil. Hans-Gerd Pauels. Internet: www.pauels-scientific.de. USt-IdNr. DE 234 757 828.

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Pauels Consulting -Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -Nonclinical Project Development - Drug Regulatory Affairs

http://www.pauels-scientific.de/index.html

Scientific Consulting, Medical Writing,. Based on broad in-house expertise and a strong network of external partners and academic experts, Pauels Consulting can assist your drug development projects from planning of early pharmacodynamic studies through the design and monitoring of pharmacokinetic and toxicological programmes, to the final compilation of MAA documents. Besides classical small molecule pharmaceuticals, Pauels Consulting focuses on biotechnology derived drugs.

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Pauels Consulting -Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -Nonclinical Project Development - Drug Regulatory Affairs

http://www.pauels-scientific.de/regulatory.html

Scientific Consulting, Medical Writing,. In identifying the optimal MAA strategy (as a Europe-based consultancy, Pauels Consulting is specialized on national, decentralised, and centralised European procedures),. Pauels Consulting can assist you. In organizing advice meetings with regulatory agencies, in preparing briefing documents and presentations, as well as preparation of meeting minutes,. In IMPD and CTD compilation (paper form as well as eCTD), and transformation of older documents into CTD format,.

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bioreg-advice.de

BioReg Consultancy - Management Consultancy for biopharmaceutical companies: Network

http://www.bioreg-advice.de/network.html

BioReg Consultancy’s international network of experts comprises:. With the main focus on development, regulatory affairs and GMP inspections for biopharmaceuticals. Pauels Consulting, Germany. With the main focus on nonclinical development of biopharmaceuticals. Pharmitas Ltd, Jon Betts, United Kingdom. With the main focus on UK manufacturing and QP batch release. Archemin bvba, Belgium. With the main focus on regulatory affairs in the Benelux region. Judy Atkins, USA.

bioreg-advice.com

BioReg Consultancy - Management Consultancy for biopharmaceutical companies: Network

http://www.bioreg-advice.com/network.html

BioReg Consultancy’s international network of experts comprises:. With the main focus on development, regulatory affairs and GMP inspections for biopharmaceuticals. Pauels Consulting, Germany. With the main focus on nonclinical development of biopharmaceuticals. Pharmitas Ltd, Jon Betts, United Kingdom. With the main focus on UK manufacturing and QP batch release. Archemin bvba, Belgium. With the main focus on regulatory affairs in the Benelux region. Judy Atkins, USA.

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pauels-scientific.de

Pauels Consulting -Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -Nonclinical Project Development - Drug Regulatory Affairs

Scientific Consulting, Medical Writing,. Based on broad in-house expertise and a strong network of external partners and academic experts, Pauels Consulting can assist your drug development projects from planning of early pharmacodynamic studies through the design and monitoring of pharmacokinetic and toxicological programmes, to the final compilation of MAA documents. Besides classical small molecule pharmaceuticals, Pauels Consulting focuses on biotechnology derived drugs.

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