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Accudata Solutions

Will your methods of data storage and preparation withstand an audit and adhere. Will your methods of data storage and preparation withstand an audit and adhere. Does your company manufacture pharmaceutical, biotechnology, or medical device products that require regulatory approval to market: (NDA, 510(k), PMA, ELA, BLA)? Ever wonder if your research designs and methods are robust, yet reasonable enough, to satisfy the regulatory process(FDA, USP, ICH)?

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Accudata Solutions | accudatasolutions.com Reviews

https://accudatasolutions.com

Will your methods of data storage and preparation withstand an audit and adhere. Will your methods of data storage and preparation withstand an audit and adhere. Does your company manufacture pharmaceutical, biotechnology, or medical device products that require regulatory approval to market: (NDA, 510(k), PMA, ELA, BLA)? Ever wonder if your research designs and methods are robust, yet reasonable enough, to satisfy the regulatory process(FDA, USP, ICH)?

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1

Accudata Solutions | Pharmaceutical Path

http://www.accudatasolutions.com/path-pharmaceutical.php

The path to marketing approval of your pharmaceutical or biologic product contains dead-ends, changes of direction, 12-foot fences, bewildering junctions, cliffs, and washouts. Unfortunately, there are no? Or other signs of warning along the way. T your company benefit from having expert advisors, guides, and negotiators with you every step of the way? From basic research to marketing submission? S successful negotiation with regulatory and reviewing bodies has meant that our clients?

2

Accudata Solutions | Pharmaceutical Path

http://www.accudatasolutions.com/path-medical-device.php

Medical Device and Diagnostic Path. The industry of medical device and diagnostic development is fast-paced. The speed of technology changes guarantees short product life cycles and a highly-competitive medical technology environment. You need an efficient guide who can help you design and analyze optimum research studies to get your product on the market faster. Mouse over a link below to find out how we can bring similar successes to your company in each of the following areas:.

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Accudata Solutions

http://www.accudatasolutions.com/index.php

Will your methods of data storage and preparation withstand an audit and adhere. Will your methods of data storage and preparation withstand an audit and adhere. Does your company manufacture pharmaceutical, biotechnology, or medical device products that require regulatory approval to market: (NDA, 510(k), PMA, ELA, BLA)? Ever wonder if your research designs and methods are robust, yet reasonable enough, to satisfy the regulatory process(FDA, USP, ICH)?

4

Accudata Solutions

http://www.accudatasolutions.com/papers.php

5

Accudata Solutions

http://www.accudatasolutions.com/testimonials.php

Biometric Research Institute -. Doug provides thoughtful analysis of protocols from a statistical perspective which are thorough and useful. Scott Stromatt, M.D. Biometric Research Institute -. Doug demonstrated a good grasp of [the]complexity of our GMP analytical methods and was able to apply a variety of statistical analysis methods to help us get the most value from our existing data. Manager of Assay Development. Elise Burmeister Getz, Ph.D. Vice President, Clinical and Medical Affairs.

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Will your methods of data storage and preparation withstand an audit and adhere. Will your methods of data storage and preparation withstand an audit and adhere. Does your company manufacture pharmaceutical, biotechnology, or medical device products that require regulatory approval to market: (NDA, 510(k), PMA, ELA, BLA)? Ever wonder if your research designs and methods are robust, yet reasonable enough, to satisfy the regulatory process(FDA, USP, ICH)?

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