Authors: Why Publish in Journal of Therapeutic Biotechnology

• No page charges(Save 5000-10, 000 $)No extra charges for colored Figures, photographs, artwork, audio or video input (saves 3000 $)
• Fast track status and priority review
• Fast peer reviewed publication by 3rd week of submission.
• A five star evaluation system
• Round the clock editorial review due to geographic location of editors.
• Open access to all articles
• Greater visibility and exposure
• Daily Page View, Comments and reviews measures Impact of your article and feedback from your audience

Priority publications supports your patents, brands and IPR

• That the submission is a new creative contribution.
• It has not been previously submitted to any other biomedical journal.
• It has not been rejected by other journals.
• The work is original and is not copied, old recycled or plagiarised material.
• All rules, regulations and guidelines were adhered to for the conduct of the studies.
• Integrity of the data was insured by the pricipal investigator.
• Conflict of interest statement.
• Contributions of all listed authors must be specified.

Citing of self references will be limited to 20% of total 25-35 (50 for review articles) references cited.

Proof of concept should be provided in simple and clear terms.

• http://www.icmje.org/

• http://mulford.meduohio.edu/instr/itoaC.php

Ethical Guidelines

World Medical Assembly Declaration of Helsinki

• http://www.wma.net/e/policy/b3.htm

• http://www.fda.gov/oc/gcp/
• http://www.ich.org/LOB/media/MEDIA482.pdf

Clinical Trials submission

All clinical trials must comply with all applicable national and international laws, rules, regulations and guidelines. Sponsors and investigators must strive to attain highest scientific, technical, analytical, medical and ethical standards.

All papers dealing with clinical trials must be accompanied by:

• International Clinical trial registry number
• Patient Informed Consent Form
• Approvals by ERC/IRB and FDA/or other national health authority
• Signed protocol + any amendments
• Payment range to investigators, labs, patients
• Patient recruitment advertisements
• Case report form
• Drop Outs/Discontinuations and serious adverse drug reactions
• Drug related laboratory changes
• Statistical methodology
• Start and end date of the trial
• Training of investigators or meetings and monitoring statement

For trials in low income countries

• Compliance with WHO ethical guidelines
• Provision for continued drug supply to all responding patients
• Statement that no bribes or undue payments were made.

Good Manufacturing Practise GMP

• http://www.fda.gov/CDRH/DEVADVICE/32.html
• http://www.ich.org/LOB/media/MEDIA433.pdf

Good laboratory Practise GLP

• http://www.oecd.org/department/0, 3355, en_2649_34381_1_1_1_1_1, 00.html

Animal Studies

• http://www.nist.gov/admin/mo/adman/1402.htm

Writers Resources

• Knols Peter Baskerville: Peter Baskerville
• How to Write an Article Review - Basic
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• Knol: Why Should You Contribute Knols
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Norman Creaney: Norman Creaney

• How to Write a Great CV (Resume)
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• Publishing your Scientific, Technical or Medical manuscript

• Amy J. Markowitz, JD
• Scientific and Medical Writing

• http://www.amwa.org
• http://www.oup.com/us/companion.websites/9780195176339/

• http://www.councilscienceeditors.org/
• http://www.councilscienceeditors.org/publications/style.cfm

• http://www.ease.org.uk/
• European Medical Writers Association : http://www.emwa.org/
• Society for Scholarly Publishing: http://www.sspnet.org/
• World Association of Medical Editors http://www.wame.org/

• http://mulford.meduohio.edu/instr/itoaC.php

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Directory of open access journals

• http://www.doaj.org/

Free Medical journals

• http://www.freemedicaljournals.com/

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