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5.Amendment to the Medicines (Applications for Product Licences and Clinical Trial and Animal Test Certificates) Regulations 1971
7.Amendment to the Medicines (Advertising of Medicinal Products) (No. 2) Regulations 1975
PARTICULARS REQUIRED IN INFORMATION SHEETS AND DATA SHEETS
1.Each purpose for which the contact lens substance is to...
2.A description of the pharmaceutical form of the contact lens...
3.The active ingredients of the contact lens substance and its...
4.The name of any antimicrobial agent which is an ingredient...
5.The quantity or amount of the contact lens substance in...
6.The compatibility and incompatibility of the contact lens substance for...
7.Possibilities of interaction between the contact lens substance and any...
9.A recommended period within which the contact lens substance should...
10.Any special requirements for the storage of the contact lens...
11.Those adverse reactions to the contact lens substance which, if...
12.Appropriate remedial measures in response to any adverse reaction to...
13.Recommendations as to the antidote to be administered or other...
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