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specific requirements for canines
specific requirements for canines
Laatste Update: 2011-10-23
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requirements for combined veterinary vaccines
requirements for combined veterinary vaccines
Laatste Update: 2011-10-23
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efficacy on anthelmintics: general requirements
efficacy on anthelmintics: general requirements
Laatste Update: 2011-10-23
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linhas de orientação requirements for combined veterinary
guidelines requirements for combined veterinary
Laatste Update: 2011-10-23
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efficacy on anthelmintics: specific requirements for canine
efficacy on anthelmintics: specific requirements for canine
Laatste Update: 2011-10-23
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field trials with veterinary vaccines requirements and controls applied to
field trials with veterinary vaccines requirements and controls applied to bovine serum (foetal or calf) used in the
Laatste Update: 2011-10-23
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"decommissioning requirements for ireland's demersal and shellfish fleets"
"decommissioning requirements for ireland's demersal and shellfish fleets"
Laatste Update: 2014-10-23
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note for guidance on requirements for pharmaceutical documentation for pressurised metered dose inhalation products
note for guidance on requirements for pharmaceutical documentation for pressurised metered dose inhalation products
Laatste Update: 2011-10-23
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harmonisation of requirements for equine influenza vaccines specific requirements for substitution or addition of a strain
harmonisation of requirements for equine influenza vaccines specific requirements for substitution or addition of a strain
Laatste Update: 2011-10-23
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points to consider on the requirements for clinical documentation for metered dose inhalers (mdi)
points to consider on the requirements for clinical documentation for metered dose inhalers (mdi)
Laatste Update: 2011-10-23
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testing of residual moisture eu requirements for batches with maximum and minimum titre or batch potency for developmental safety
testing of residual moisture eu requirements for batches with maximum and minimum titre or batch potency for developmental safety and efficacy studies
Laatste Update: 2011-10-23
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ich q1f stability data package for registration in climatic zones iii and iv requirements for pharmaceutical documentation for pressurised metered dose inhalation products
ich q1f stability data package for registration in climatic zones iii and iv requirements for pharmaceutical documentation for pressurised metered dose inhalation products
Laatste Update: 2011-10-23
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título field trials with veterinary vaccines requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products
dokumenttitel field trials with veterinary vaccines requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products
Laatste Update: 2011-10-23
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título antimicrobials for general use in target animal species summary of product characteristics for antimicrobial products efficacy requirements for ectoparasiticides for cattle fluid therapy
dokumenttitel antimicrobials for general use in target animal species summary of product characteristics for antimicrobial products efficacy requirements for ectoparasiticides for cattle fluid therapy
Laatste Update: 2011-10-23
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position paper on the regulatory requirements for the authorisation of low- dose modified release asa formulations in the secondary prevention of cardiovascular events.
position paper on the regulatory requirements for the authorisation of low- dose modified release asa formulations in the secondary prevention of cardiovascular events.
Laatste Update: 2011-10-23
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note for guidance on the use of bovine serum in the manufacture of human biological medicinal products concept paper on the development of a cpmp note for guidance on requirements for the evaluation of new adjuvants in vaccines
concept paper on the development of a cpmp note for guidance on requirements for the evaluation of new adjuvants in vaccines
Laatste Update: 2011-10-23
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countries and establishments complying with all requirements of article 2(1) of council decision 95/408/ec.
countries and establishments complying with all requirements of article 2(1) of council decision 95/408/ec.
Laatste Update: 2014-10-23
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however, this condition is insufficient to comply with the requirements established in point 2.2.3.3. of the 1994, the 1997 as well as the 2001 guidelines.
however, this condition is insufficient to comply with the requirements established in point 2.2.3.3. of the 1994, the 1997 as well as the 2001 guidelines.
Laatste Update: 2014-10-23
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note for guidance on cell culture inactivated influenza vaccines – annex to note for guidance on harmonisation of requirements for influenza vaccines cpmp/ bwp/ 214/ 96
note for guidance on cell culture inactivated influenza vaccines – annex to note for guidance on harmonisation of requirements for influenza vaccines cpmp/ bwp/ 214/ 96
Laatste Update: 2011-10-23
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título requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products eu requirements for batches with maximum and minimum titre or batch potency for developmental safety and efficacy studies requirements for live recombinant vectored vaccines requirements for compatibility statements for veterinary vaccines harmonisation of requirements for potency and batch consistency of vaccines vich:
dokumenttitel requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products eu requirements for batches with maximum and minimum titre or batch potency for developmental safety and efficacy studies requirements for live recombinant vectored vaccines requirements for compatibility statements for veterinary vaccines harmonisation of requirements for potency and batch consistency of vaccines vich:
Laatste Update: 2011-10-23
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