Clinical Trial Advice |
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Dedicated Clinical Trial Administrator |
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SCGF will dedicate an administrator to your clinical trial.
That way you always have someone you can talk to who understands YOUR trial. All our clinical trial administrators will be trained under GXP (GCP, GMP & GDP) and have a good grounding in clinical research. |
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Confidential Troubleshooting |
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SCGF’s team of experts can help you get your trial back on track
Are you having problems with your clinical trial?
Is it taking ages to get up and running?
Perhaps you have a trial which is not recruiting or has suddenly stalled?
Whether you are a Chief Executive Officer looking to deliver your trial results to city investors or a Clinical Research Associate working for a large CRO, you can talk to us in absolute confidence. |
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Patient Recruitment Acceleration & Retention |
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SCGF understands the pressure to deliver trials on time.
Identifying, recruiting and maintaining your patient cohort is crucial to the timely completion of any clinical trial, large or small. Rapid patient recruitment is vital for new products requiring regulatory clearance and just as important for marketing current products.
Not only can SCGF help you speed up patient recruitment and retain patients in stalling trials, they can also help you avoid pitfalls in future trials. |
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Blinding and Randomization |
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Let SCGF take care of all your blinding and randomization needs...
What is blinding?
Blinding means that the treatment a patient receives in a clinical trial is hidden from the patient themselves.
Single Blinding means that the patient does not know which treatment they are receiving but the medical team treating the patient are aware.
Double Blinding means that neither the patient nor the medical team knows what treatment the patient is receiving.
SCGF can take care of these complicated procedures on your behalf. A 24 hour code break telephone line or code break envelope will be provided in case of emergency to inform the doctors of the treatment the patient is receiving.
What is Randomization?
Randomization is the use of probability (random number generation) to allocate a patient to a particular treatment or control group.
SCGF can take care of this on your behalf, freeing up time in your trial. |
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Regulatory Support |
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Rapid Ethics Submissions |
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Take Ethics in your stride with SCG...
Ethics are an important and essential part of the clinical trials process. If you are finding the Ethics Form a hurdle or perhaps you are just struggling with one part of the form, let SCGF’s friendly team of expert’s guide you through the form and the application process, with as much or as little help as you need.
We can also help you meet the Ethics deadline, prepare for the Ethics meeting if required and help you answer any Ethics Committee queries rapidly. |
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Protocol Creation & Translation |
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Give the best impression, work with SCGF.
A good protocol is an essential document for everyone involved in a clinical trial. A clear and concise protocol will help you speed through your ethics and other regulatory submissions and save you valuable time so that your clinical trial will run smoothly and to plan.
If medical teams can easily follow the protocol, and in turn conform to it, there will be fewer protocol violations when the clinical data is gathered at the end of the trial. If you are daunted by writing your protocol and do not know where to start please contact us for further advice. We already have a portfolio of tried and tested protocol formats which we can make available to you so that your trial looks just as professional as the most prestigious clinical trials in the industry. |
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Clinical trial logistics |
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Clinical Trial Storage |
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Running short on space?
Would your hospital like to take on more clinical trials but you do not have the storage capacity?
Is your hospital getting overcrowded by clinical trial supplies?
Are you having difficulty finding specific trial products on your shelves?
SCGF can provide the solution. With bespoke clinical storage facilities we can hold as much or as little of your clinical trial stock as you need and then release it as and when you and your patients require it.
If this sounds far too complicated you will be pleased to hear that...
SCGF can facilitate the smooth importation and distribution of clinical trials to and from countries all around the world - particularly relevant when administering major clinical trials |
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Labeling, Packaging & Distribution |
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Labeling is crucial to the success of clinical trials and inappropriate label design issues are often cause for concern with regulatory authorities and can hinder a trial's progress.
In line with GCP and GMP requirements, our experienced bank of clinical labeling specialists can design, generate and apply all the clinical trial labels you require, in whatever language you need, at a competitive cost and with a rapid turnaround time.
SCGF ensures that your clinical trial supplies are carefully stored, wrapped, packed, cushioned and transported, with temperature regulation where appropriate.
We care about your clinical trial product as much as you do and we will ensure that you receive the high quality service you expect, so that you can deliver your clinical trial supplies to your partners on time.
So, for any kind of support required in regards of Multicentric Stem Cell Clinical trials, contact SCGF. |
