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Obtaining approval to market a new drug is an expensive, complex, and lengthy process. A critical element of this process is the medical writing needed to meet regulatory requirements. Throughout my career I have worked with challenging time lines to get the job done. I thoroughly comprehend the complex problems associated with preparation of regulatory submissions, and can provide quality, rapid turn-around for your clinical writing projects. ClinDoc Associates, Ltd.

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ClinDoc Associates, Ltd.

Linda Puertolas

907 W●●●●●ow Ct

C●y , North Carolina, 27513

United States

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ClinDoc Associates, Ltd.

Linda Puertolas

907 W●●●●●ow Ct

C●y , North Carolina, 27513

United States

1.91●●●●4682
1.91●●●●0754
cl●●●●●@bellsouth.net

View this contact

ClinDoc Associates, Ltd.

Linda Puertolas

907 W●●●●●ow Ct

C●y , North Carolina, 27513

United States

1.91●●●●4682
1.91●●●●0754
cl●●●●●@bellsouth.net

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ClinDoc Home Page | clindoc.net Reviews
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Obtaining approval to market a new drug is an expensive, complex, and lengthy process. A critical element of this process is the medical writing needed to meet regulatory requirements. Throughout my career I have worked with challenging time lines to get the job done. I thoroughly comprehend the complex problems associated with preparation of regulatory submissions, and can provide quality, rapid turn-around for your clinical writing projects. ClinDoc Associates, Ltd.
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1 clindoc
2 FDA
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6 Medical writing services
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8 drug reports
9 drug studies
10 contract writing services
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ClinDoc Home Page | clindoc.net Reviews

https://clindoc.net

Obtaining approval to market a new drug is an expensive, complex, and lengthy process. A critical element of this process is the medical writing needed to meet regulatory requirements. Throughout my career I have worked with challenging time lines to get the job done. I thoroughly comprehend the complex problems associated with preparation of regulatory submissions, and can provide quality, rapid turn-around for your clinical writing projects. ClinDoc Associates, Ltd.

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ClinDoc Experience

http://www.clindoc.net/newTAs.html

Therapeutic area experience includes:. Infectious Disease: Skin, urinary tract, sexually transmitted, and upper and lower respiratory tract infections. Central Nervous System: Stroke, schizophrenia, epilepsy, Alzheimer's disease, Restless Legs Syndrome, and analgesia. Rheumatology: Osteoarthritis, Rheumatoid arthritis. Urology: Benign prostatic hyperplasia, Bladder over activity.

2

ClinDoc Home FAQs

http://www.clindoc.net/newfaq.html

Why contract medical writing services? Obtaining approval to market a new drug is an expensive, complex, and lengthy process. A critical element of this process is the medical writing needed to meet regulatory requirements. In the fast-paced world of the pharmaceutical industry, clinical researchers must efficiently:. Comply with all regulatory guidelines. Employ cost saving methods. Produce skillfully prepared documents. Why choose ClinDoc Associates, Ltd? Pay attention to detail. Think on my feet.

3

ClinDoc Experience

http://www.clindoc.net/newexperience.html

Experience since 1990 as a medical writer specializing in clinical and regulatory documents supporting New Drug Applications (Hoffmann-La Roche Inc., R.W. Johnson Pharmaceutical Research Institute, and Glaxo Wellcome Inc.). Two years as a Clinical Research Associate monitoring clinical and clinical pharmacology trials and designing protocols and case report forms (Hoffmann-La Roche Inc.). EdM Degree in Education from Rutgers University. New Brunswick, NJ. BA Degree in Psychobiology, State.

4

ClinDoc Home FAQs

http://www.clindoc.net/newservice.html

Provide medical writing services including preparation of clinical documentation for regulatory submissions across various therapeutic areas:. Clinical Study Reports (Phase I to IV). Integrated Summary Documents (ISS, ISE).

5

ClinDoc Home Page

http://www.clindoc.net/index.html

Obtaining approval to market a new drug is an expensive, complex, and lengthy process. A critical element of this process is the medical writing needed to meet regulatory requirements. Throughout my career I have worked with challenging time lines to get the job done. I thoroughly comprehend the complex problems associated with preparation of regulatory submissions, and can provide quality, rapid turn-around for your clinical writing projects. ClinDoc Associates, Ltd.

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Obtaining approval to market a new drug is an expensive, complex, and lengthy process. A critical element of this process is the medical writing needed to meet regulatory requirements. Throughout my career I have worked with challenging time lines to get the job done. I thoroughly comprehend the complex problems associated with preparation of regulatory submissions, and can provide quality, rapid turn-around for your clinical writing projects. ClinDoc Associates, Ltd.

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