I am trying to generate the SSRS report in AWDOC format. When I have below text it works fine. but as soon as I add other two lines it does not generate the report. I tried adding other text then it works fine. any issue with text format or something ? Please help.
Below works fine
A Site Specific Amendment to update the Adult and Parental
Informed Consent Forms, to add a new Investigator Samuel G. Ouma and to updated
the Site Specific Addendum with details of Pharmacokinetic (PK) Sampling for
participants on Efavirenz and Nevirapine
was submitted to ECCT at PPB in a letter dated 18/Nov/2014. Submitted
documents were the same as those submitted to the KEMRI ERC along with evidence
of ERC approval. Approval was granted in a letter dated 27/Jan/2015.
Request for annual approval was submitted to the Regulatory Authority, the Expert Committee on Clinical Trials (ECCT) at the Pharmacy and Poisons Board (PPB). Submitted documents include:
- Protocol Version 2.0 dated 28/Aug/2014
- Site Specific Addendum Version 1.5 dated 24/Nov/2014
- English, Swahili and Luo Informed Consent Forms Version 1.2 dated 08/Jan/2015
- English, Swahili and Luo Informed Assent Forms Version 1.2 dated 08/Jan/2015
- English, Swahili and Luo Parental Consent Forms Version 1.2 dated 08/Jan/2015
- Study Information Sheet Version 1.2 dated 08/Jan/2015
- Translations
- Package Inserts for Rifapentine, Isoniazid and Pyridoxine
- Letters of Amendment 1, 2, 3 and 4
Approval was granted in a letter dated 04/Jun/2015. Expiry period noted as one year from the date of approval.
Protocol Version 2.0 dated 28/Aug/2014 was submitted to the ECCT at PPB. Submitted documents include:
- Protocol Version 2.0 dated 28/Aug/2014
- Site Specific Addendum Version 1.5 dated 24/Nov/2014
- English, Swahili and Luo Informed Consent Forms Version 1.2 dated 08/Jan/2015
- English, Swahili and Luo Informed Assent Forms Version 1.2 dated 08/Jan/2015
- English, Swahili and Luo Parental Consent Forms Version 1.2 dated 08/Jan/2015
- Study Information Sheet Version 1.2 dated 08/Jan/2015
- Letters of Amendment 1, 2, 3 and 4
Below does not work
A Site Specific Amendment to update the Adult and Parental Informed Consent Forms, to add a new Investigator Samuel G. Ouma and to updated the Site Specific Addendum with details of Pharmacokinetic (PK) Sampling for participants on Efavirenz and Nevirapine was submitted to ECCT at PPB in a letter dated 18/Nov/2014. Submitted documents were the same as those submitted to the KEMRI ERC along with evidence of ERC approval. Approval was granted in a letter dated 27/Jan/2015.
Request for annual approval was submitted to the Regulatory Authority, the Expert Committee on Clinical Trials (ECCT) at the Pharmacy and Poisons Board (PPB). Submitted documents include:
- Protocol Version 2.0 dated 28/Aug/2014
- Site Specific Addendum Version 1.5 dated 24/Nov/2014
- English, Swahili and Luo Informed Consent Forms Version 1.2 dated 08/Jan/2015
- English, Swahili and Luo Informed Assent Forms Version 1.2 dated 08/Jan/2015
- English, Swahili and Luo Parental Consent Forms Version 1.2 dated 08/Jan/2015
- Study Information Sheet Version 1.2 dated 08/Jan/2015
- Translations
- Package Inserts for Rifapentine, Isoniazid and Pyridoxine
- Letters of Amendment 1, 2, 3 and 4
Approval was granted in a letter dated 04/Jun/2015. Expiry period noted as one year from the date of approval.
Protocol Version 2.0 dated 28/Aug/2014 was submitted to the ECCT at PPB. Submitted documents include:
- Protocol Version 2.0 dated 28/Aug/2014
- Site Specific Addendum Version 1.5 dated 24/Nov/2014
- English, Swahili and Luo Informed Consent Forms Version 1.2 dated 08/Jan/2015
- English, Swahili and Luo Informed Assent Forms Version 1.2 dated 08/Jan/2015
- English, Swahili and Luo Parental Consent Forms Version 1.2 dated 08/Jan/2015
- Study Information Sheet Version 1.2 dated 08/Jan/2015
- Letters of Amendment 1, 2, 3 and 4
Approval was granted in a letter dated 13/May/2015. Approval period noted as 13/May/2015 to 12/May/2016.
Please help.