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A newsletter for those involved in clinical trials. Published 20 times a
year by Canary LtdPatient information
The following articles on this topic have been published in
CRAdvisor (CRA) – the year, issue number
and starting page number for each are listed below:
Back to index |
| 2007 |
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CRA 2007; 183:6 |
EMEA launches EudraPharm, the European medicines database. |
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CRA 2007; 185:6 |
Guidance on consent and information sheets. |
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| 2006 |
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CRA 2006; 163:5 |
IRB review of clinical trial websites. |
| CRA 2006; 163:6 |
Results of survey into on-line clinical trials registries. |
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CRA 2006; 169:2 |
EC issues revised Detailed Guidance on ethics committee applications. |
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CRA 2006; 170:8 |
Pharmaceutical industry restricts trial information being made public. |
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CRA 2006; 171:5 |
IRBs violate FDA regulations. |
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CRA 2006; 173:5 |
On-line trial registries are not enough. |
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CRA 2006; 182:11 |
Consumers for Ethics in Research to disband this month. |
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CRA 2006; 182:11 |
PhRMA launches campaign to improve cancer awareness. |
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| 2005 |
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| CRA 2005; 152:1 |
International trials database for patients and doctors in
action by September 2005. |
| CRA 2005; 152:6 |
EMEA publishes final recommendations on working with
Patients Organisations. |
| CRA 2005; 153:6 |
Industries' clinical trial registries. |
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| 2004 |
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| CRA 2004; 126:7 |
Better information for patients. |
| CRA 2004; 132:4 |
Independent contact point in The Netherlands has to be
physician. |
| CRA 2004; 134:6 |
Who should be the contact point for subjects enrolled in
trials? |
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| 2003 |
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| CRA 2003; 120:7 |
Consumer information sheets on the Internet. |
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| 2002 |
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| CRA 2002; 85:1 |
Subjects do not understand study information. |
| CRA 2002; 89:3 |
Consent in pharmacogenetics. |
| CRA 2002; 91:1 |
EMEA workshop for patients' organisations. |
| CRA 2002; 92:1 |
Direct contact with patients wanted. |
| CRA 2002; 93:4 |
Patients want more direct information: EU set to change
rules. |
| CRA 2002; 94:2 |
Guidance for Ethics Committee applications. |
| CRA 2002; 101:3 |
Parliament vote against direct information to patients. |
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| 2001 |
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| CRA 2001; 65:1 |
New patient information sheet guidelines for UK. |
| CRA 2001;65:sup |
Guidelines for researchers : patient information sheet and
consent form guidelines. |
| CRA 2001; 72:6 |
Clearer patient information is still required! |
| CRA 2001; 78:3 |
Patient information sheet omits safety data. |
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| 2000 |
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| CRA 2000; 40:6 |
Do patients understand? |
| CRA 2000; 49:6 |
Patient information sheet guidelines in Greece. |
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| 1999 |
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| CRA 1999; 20:3 |
US version of patient information template. |
| CRA 1999; 23:1 |
Patient information template nears completion. |
| CRA 1999; 27:1 |
Patient information sheet may eliminate Ethics Committee
delays. |
| CRA 1999; 27:1 |
Europe needs PINF guidelines too. |
| CRA 1999; 27:3 |
Guidelines for researchers – patient information sheet and
consent form. |
| CRA 1999; 29:4 |
Declaration of Ottawa protects children. |
| CRA 1999; 30:1 |
Sponsor will be responsible for independent contact point.
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| CRA 1999; 31:4 |
Patient information sheets for children. |
| CRA 1999; 32:1 |
Compensation rights – are patients aware? |
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| 1998 |
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| CRA 1998; 6:2 |
Guidance on patient information and consent forms.
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| CRA 1998; 8:1 |
Patients will need independent trial information.
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| CRA 1998; 10:1 |
UK releases template for standard patient information
sheet. |
| CRA 1998; 10:1 |
All risks or just some risks? |
| CRA 1998; 10:sup |
Taking part in research. |
| CRA 1998; 16:4 |
Progress towards a standard patient information sheet.
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