DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

More documents

Recommendations

Info

Drug Registration Guidance Document (DRGD)5.2.5 APPLICATION FOR A CONVENIENT PACKa) Refers to products which are packed together in a single packaging unitfor convenience of the consumers, such as a Confinement Set or SetJamu Bersalin.b) Shall consist of registered products only.c) Applicable to health supplements and natural products only.d) Application for a convenient pack shall be made via the variation process.For details, please refer to Section E: 16.1 Variation and Section E: 16.5Application for a Convenient Pack.5.3 RENEWAL OF PRODUCT REGISTRATIONThe registration shall be valid for five (5) years or such a period as specified in theregistration certificate (unless sooner suspended or cancelled by the Authority);The renewal of product registration should be done not later than 6 month prior to expirytogether with appropriate fee.Please refer also at Section E: 14 Maintenance of Registration.5.4 CERTIFICATES5.4.1 CERTIFICATE OF PHARMACEUTICAL PRODUCT (CPP)A CPP which follows the format recommended by WHO shall be issued to locallymanufactured products that are to be exported. For application of CPP, applicantshall fill in form BPFK 412.2: Permohonan Perakuan Keluaran Farmaseutikal.A fee, as stated in Appendix 1: Fees, is payable on the issue of such certification.Upon receipt of complete application, the certificate shall be issued within fifteen (15)working days.National Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 62
Drug Registration Guidance Document (DRGD)5.4.2 GOOD MANUFACTURING PRACTICE (GMP) CERTIFICATEAccording to the CDCR 1984, compliance to Good Manufacturing Practice (GMP) isprerequisite to application of a manufacturing license, as well as product registration/cosmetic notification.GMP is a standard which shall be followed by the manufacturers to ensure that theproducts manufactured are safe, efficacious and of quality.Upon complete application, a GMP certificate will be issued and a fee, as stated inAppendix 1: Fees, is payable on the issue of such certification.If a manufacturer who wishes to build a new manufacturing premise, themanufacturer may submit a proposed premise layout plan to the Centre forCompliance and Licensing, NPCB for evaluation.For more information, please refer Section D: 13.4 GMP Certificate and/or NPCBwebsite.5.5 LICENSESNote:In addition to the relevant laws and regulations as stated in this DRGD,manufacturers are required to comply with the principles of Good ManufacturingPractice (GMP) and Good Distribution Practice (GDP). Meanwhile, Importers andWholesalers are required to comply with the principles of Good Distribution Practice(GDP).According to the CDCR 1984, any company who wishes to manufacture, import and/orwholesale any registered products needs to have Manufacturer‟s Licence, Import Licenceand/or Wholesaler‟s License.For more information pertaining application of appropriate licences, please refer Section D:13. Licensing or contact Licensing Unit, Centre for Compliance and Licensing (CCL), NPCBor NPCB website.As for processing fee for these applications, please refer to Appendix 1: FeesNational Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 63
Page 2 and 3:
Drug Registration Guidance Document
Page 5 and 6:
Page 7 and 8:
Page 9 and 10:
Page 11 and 12: Drug Registration Guidance Document
Page 31: Drug Registration Guidance Document
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:
Appearance/organoleptic(odor, color
Page 198 and 199:
Page 200 and 201:
Page 202 and 203:
Page 204 and 205:
Page 206 and 207:
Page 208 and 209:
Page 210 and 211:
Page 212 and 213:
Page 214 and 215:
ATTACHMENT 1Drug Registration Guida
Page 216 and 217:
Page 218 and 219:
Page 220 and 221:
Page 222 and 223:
PART IV: CLINICAL DOCUMENTSDrug Reg
Page 224 and 225:
ATTACHMENT 2Drug Registration Guida
Page 226 and 227:
Page 228 and 229:
Page 230 and 231:
APPENDIX 5:Drug Registration Guidan
Page 232 and 233:
1. GENERAL INFORMATIONSDrug Registr
Page 234 and 235:
Page 236 and 237:
Page 238 and 239:
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:
Route of AdministrationTAMC(CFU/g o
Page 270 and 271:
Page 272 and 273:
Page 274 and 275:
Page 276 and 277:
d) Example of label approved by the
Page 278 and 279:
Page 280 and 281:
Page 282 and 283:
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:
Page 386 and 387:
Page 388 and 389:
Page 390 and 391:
Page 392 and 393:
Page 394 and 395:
Page 396 and 397:
Page 398 and 399:
Page 400 and 401:
Page 402 and 403:
Page 404 and 405:
Page 406 and 407:
Page 408 and 409:
Page 410 and 411:
Page 412 and 413:
Page 414 and 415:
Page 416 and 417:
Page 418 and 419:
Page 420 and 421:
Page 422 and 423:
Page 424 and 425:
Page 426 and 427:
Page 428 and 429:
Page 430 and 431:
Page 432 and 433:
Page 434 and 435:
Page 436 and 437:
Page 438 and 439:
Page 440 and 441:
Page 442 and 443:
Page 444 and 445:
Page 446 and 447:
Page 448 and 449:
Page 450 and 451:
Page 452 and 453:
Page 454 and 455:
Page 456 and 457:
Page 458 and 459:
Page 460 and 461:
Page 462 and 463:
Page 464 and 465:
Page 466 and 467:
Page 468 and 469:
Page 470 and 471:
Page 472 and 473:
Page 474 and 475:
Page 476 and 477:
Page 478 and 479:
Page 480 and 481:
Page 482 and 483:
Page 484 and 485:
Page 486:
show all

DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

Create successful ePaper yourself

Delete template?

Save as template?