DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

More documents

Recommendations

Info

Drug Registration Guidance Document (<strong>DRGD</strong>)11.1 PRODUCT CLASSIFICATIONApplicant shall ensure correct product category as listed below in order to determinethe method of evaluation i.e. full evaluation (*) or abridged evaluation (**) in whichavailable as separate modules for application.11.1.1 Pharmaceuticalsi) New Drug Products *ii) Biologicals *iii) Generics (Scheduled Poison) *iv) Generics (Non-Scheduled Poison) (or known as OTC/ non-prescription) -other than listed at v) *v) Generics (Non-Scheduled Poison) **, which include, but not limited to thefollowing:Antiseptics/ skin disinfectants;Locally-acting lozenges/ pastilles;Topical analgesic/ counter-irritants;Topical nasal decongestants;Emollient/ demulcent/ skin protectants;Keratolytics;Anti-dandruff;Oral care;Anti-acne;Medicated plasters/ patch/ pad; andTopical antibacterial.11.1.2 Health Supplements and Natural Products **Application form for registration for Health Supplements; and Natural Products(or termed as Traditional Products) are available under Abridged module.Do not use the pharmaceuticals module for these product categories.11.2 SUBMISSION OF APPLICATIONAny application for a product registration shall follow a 2-step process i.e. Step 1(Product Validation) and Step 2, as described below:National Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 434
Drug Registration Guidance Document (<strong>DRGD</strong>)11.2.1 STEP 1: PRODUCT VALIDATIONAll fields are compulsory to be entered.Option is given either to accept the validation result and submit; or overrideand manually select.Once validation is verified and submitted, the related application form underStep 2 will be displayed.Information entered in Step 1 will be captured in the database and need notbe re-entered at Step 2.[1] Product NameProduct name, dosage form and strength shall be entered.(e.g. X Brand Paracetamol Tablet 500mg)Product name is defined as a name given to a product which may beeither a proprietary name (an invented name); or a generic name(common name) or scientific name, together with a trade mark or thename of the manufacturer.Product name shall not imply the following:a. Tricky, confusive and against the law;b. Scandalous and offensive;c. Prejudicial;d. Notorious.Any product name which is the same or similar either in writing/pronunciation, with the product name of an adulterated product or aproduct that has been revoked due to safety concerns is prohibited.The invented name shall not be liable to confusion with the commonname.The generic name means the international non-proprietary namerecommended by WHO (rINN), or if one does not exist, the usualapproved name.The product name shall be shown on the product labelling i.e. immediatelabel, outer unit carton, package insert and patient information leaflet.Dosage form and strength of product would need to be entered as part ofproduct name to allow for multiple dosage forms (e.g. tablet, capsule) andstrengths (e.g. 200mg and 400mg) for any particular named (proprietary orgeneric) product.If a product name is found similar to another registered product or anyother name which deemed inappropriate by the Authority, NPCB reservesthe rights to request for the change of the product name.National Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 435
Page 1 and 2:
Drug Registration Guidance Document
Page 3 and 4:
Page 5 and 6:
Page 7 and 8:
Page 9 and 10:
Page 11:
Page 16 and 17:
Page 18 and 19:
Page 20 and 21:
Page 22 and 23:
Page 24 and 25:
Page 26 and 27:
Page 28 and 29:
Page 30 and 31:
Page 32 and 33:
Page 34 and 35:
Page 36 and 37:
Page 40 and 41:
Page 42 and 43:
Page 44 and 45:
Page 46 and 47:
Page 48 and 49:
Page 50 and 51:
Page 52 and 53:
Page 54 and 55:
Page 56 and 57:
Page 58 and 59:
Page 60 and 61:
Page 62 and 63:
Page 64 and 65:
Page 66 and 67:
Page 68 and 69:
Page 70 and 71:
Page 72 and 73:
Page 74 and 75:
Page 76 and 77:
Page 78 and 79:
Page 80 and 81:
Page 82 and 83:
Page 84 and 85:
Page 86 and 87:
Page 88 and 89:
Page 90 and 91:
Page 92 and 93:
Page 94 and 95:
Page 96 and 97:
Page 98 and 99:
Page 100 and 101:
Page 102 and 103:
Page 104 and 105:
Page 106 and 107:
Page 108 and 109:
Page 110 and 111:
Page 112 and 113:
Page 114 and 115:
Page 116 and 117:
Page 118 and 119:
Page 120 and 121:
Page 122 and 123:
Page 124 and 125:
Page 126 and 127:
Page 128 and 129:
Page 130 and 131:
Page 132 and 133:
Page 134 and 135:
Page 136 and 137:
Page 138 and 139:
Page 140 and 141:
Page 142 and 143:
Page 144 and 145:
Page 146 and 147:
Page 148 and 149:
Page 150 and 151:
Page 152 and 153:
Page 154 and 155:
Page 156 and 157:
Page 158 and 159:
Page 160 and 161:
Page 162 and 163:
Page 164 and 165:
Page 166 and 167:
Page 168 and 169:
Page 170 and 171:
Page 172 and 173:
Page 174 and 175:
Page 176 and 177:
Page 178 and 179:
Page 180 and 181:
Page 182 and 183:
Page 184 and 185:
Page 186 and 187:
Page 188 and 189:
Page 190 and 191:
Page 192 and 193:
Page 194 and 195:
Page 196 and 197:
Page 198 and 199:
Page 200 and 201:
Page 202 and 203:
Appearance/organoleptic(odor, color
Page 204 and 205:
Page 206 and 207:
Page 208 and 209:
Page 210 and 211:
Page 212 and 213:
Page 214 and 215:
Page 216 and 217:
Page 218 and 219:
Page 220 and 221:
ATTACHMENT 1Drug Registration Guida
Page 222 and 223:
Page 224 and 225:
Page 226 and 227:
Page 228 and 229:
PART IV: CLINICAL DOCUMENTSDrug Reg
Page 230 and 231:
ATTACHMENT 2Drug Registration Guida
Page 232 and 233:
Page 234 and 235:
Page 236 and 237:
APPENDIX 5:Drug Registration Guidan
Page 238 and 239:
1. GENERAL INFORMATIONSDrug Registr
Page 240 and 241:
Page 242 and 243:
Page 244 and 245:
Page 246 and 247:
Page 248 and 249:
Page 250 and 251:
Page 252 and 253:
Page 254 and 255:
Page 256 and 257:
Page 258 and 259:
Page 260 and 261:
Page 262 and 263:
Page 264 and 265:
Page 266 and 267:
Page 268 and 269:
Page 270 and 271:
Page 272 and 273:
Page 274 and 275:
Route of AdministrationTAMC(CFU/g o
Page 276 and 277:
Page 278 and 279:
Page 280 and 281:
Page 282 and 283:
e) Example of label approved by the
Page 284 and 285:
Page 286 and 287:
Page 288 and 289:
Page 290 and 291:
Page 292 and 293:
Page 294 and 295:
Page 296 and 297:
Page 298 and 299:
Page 300 and 301:
Page 302 and 303:
Page 304 and 305:
Page 306 and 307:
Page 308 and 309:
Page 310 and 311:
Page 312 and 313:
Page 314 and 315:
Page 316 and 317:
Page 318 and 319:
Page 320 and 321:
Page 322 and 323:
Page 324 and 325:
Page 326 and 327:
Page 328 and 329:
Page 330 and 331:
Page 332 and 333:
Page 334 and 335:
Page 336 and 337:
Page 338 and 339:
Page 340 and 341:
Page 342 and 343:
Page 344 and 345:
Page 346 and 347:
Page 348 and 349:
Page 350 and 351:
Page 352 and 353:
Page 354 and 355:
Page 356 and 357:
Page 358 and 359:
Page 360 and 361:
Page 362 and 363:
Page 364 and 365:
Page 366 and 367:
Page 368 and 369:
Page 370 and 371:
Page 372 and 373:
Page 374 and 375:
Page 376 and 377:
Page 378 and 379:
Page 380 and 381:
Page 382 and 383:
Page 384 and 385: Drug Registration Guidance Document
Page 484 and 485:
Page 486 and 487:
Page 488 and 489:
Page 490 and 491:
Page 492 and 493:
Page 494 and 495:
Page 496 and 497:
Page 498 and 499:
Page 500:
show all

DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

Create successful ePaper yourself

Delete template?

Save as template?