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GCPinfo - Clinical Trial Consultancy - Risk Based Monitoring

Clinical Trial Consultancy on Risk Based Monitoring. Our consultant help you save costs while improving the quality of clinical trial monitoring.

http://www.gcpinfo.com/

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Clinical Trial Consultancy on Risk Based Monitoring. Our consultant help you save costs while improving the quality of clinical trial monitoring.
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GCPinfo - Clinical Trial Consultancy - Risk Based Monitoring | gcpinfo.com Reviews

https://gcpinfo.com

Clinical Trial Consultancy on Risk Based Monitoring. Our consultant help you save costs while improving the quality of clinical trial monitoring.

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gcpinfo.com gcpinfo.com
1

GCPinfo - Links to important clinical trial and GCP news, information and guidelines

http://www.gcpinfo.com/links.html

FDA on Risk Based Monitoring. EMA on Risk Based Monitoring. FDA Guidance and Information. EMA Clinical Trials Guidelines.

2

GCPinfo - GCP information

http://www.gcpinfo.com/about.html

A proven track-record of Risk-Based Monitoring plan development, implementation and execution. Experience with on-site monitoring, site management and centralized monitoring – all critical items in Risk-Based Monitoring. Very Cost-efficient consultancy and money back garantee- if you are not satisfied with our work you get your money back. GCPinfo.com Clinical Trial Consultancy is headed by Jeppe R. Andersen, MSc. Pharm.

3

GCPinfo - Clinical Trial and GCP News - Stay Updated on Clinical Trials and GCP

http://www.gcpinfo.com/news.html

Clinical Trials News from the FDA Clinical Trials Advisor. Clinical Trial News from Drugs.com.

4

GCPinfo - Our Services

http://www.gcpinfo.com/services.html

How can we help You? We offer consultancy via phone, skype, email or face-to-face depending on your preference. We can help you design and implement a Risk-Based Monitoring Plan. We can provide anything from consultancy to assist you in the development of your Risk-Based Monitoring Plan or take project manager ownership of the project in collaboration with your CRA and DM team. You decide how much involvement from us you require. Feel free to Contact Us.

5

GCPinfo - FAQ - Questions and answers about Clinical Trials, Research and GCP

http://www.gcpinfo.com/faq.html

1 Why implement Risk-Based Monitoring? 2 What is Risk-Based Monitoring? 3 Advantages of Risk-Based Monitoring over "Classic" monitoring. Improved Quality and Integrity of critical data. Tailored monitoring plan to the specific study based on risk assessments. Improved quality of monitoring. Proactive rather than Reactive monitoring. Avoidance of inefficient practices that consumes valuable resources. Regulatory - USA specific. 1 How Do I Register Clinical Trials with The FDA? 3 Who must be listed on the ...

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GCPinfo - Clinical Trial Consultancy - Risk Based Monitoring

GCPinfo is Clinical Trial Consultancy for Pharma, CRO and Biotech looking to implement or improve their Risk Based Monitoring approach to save costs while improving the quality of clinical trial monitoring. Our core competencies are Clinical Trial Management and Monitoring, in particular Risk-Based Monitoring. We can provide cost-efficient consultancy to help you save up to 50% on your monitoring budgets and improve the quality of the clinical data in the process. Located in Copenhagen, Denmark.

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