DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

More documents

Recommendations

Info

Drug Registration Guidance Document (DRGD)Product registration holders are required to monitor and report any product safetyissues that arises locally or internationally to the NPCB and comply with all safetyrelateddirectives issued by the Authority.The product registration may be cancelled if the product registration holder fails toinform the Authority of any serious adverse reactions upon receipt of such reports.The WHO encourages reporting of ALL adverse drug reactions.For further information, please refer Malaysian Guidelines for the Reporting &Monitoring.17.2 POST-MARKET SURVEILLANCEa) Samples of products registered by the Authority may be taken and tested forcompliance with official or pharmacopoeia standards or specifications agreed by themanufacturer;b) If a sample fails to meet adequate specifications, the product registration holder willbe issued a warning. Unless the failure is serious enough to justify recall of theproduct, the product registration holder has up to thirty (30) days to identify thesource/ cause of quality defect and actions to be taken to improve quality.17.2.1 PRODUCT COMPLAINTSa) The product registration holder should notify the Director of PharmaceuticalServices of any product quality related problems (with registered products) thatthe holder is aware of;b) It is also the responsibility of the prescribers, the pharmacists, as well as all otherhealth professionals who come into contact with the drug to report.17.2.2 PRODUCT RECALLSa) Recalls of defective or unsafe products are instituted by the Authority, supportedby the Pharmaceutical Services Division, Ministry of Health Malaysia;National Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 118
Drug Registration Guidance Document (DRGD)b) The product registration holder is responsible for conducting recalls of defectiveor unsafe products. No recall should take place without first consulting/ informingthe Director of Pharmaceutical Services.17.3 PUNITIVE ACTION FROM THE AUTHORITY17.3.1 ADULTERATIONAs stated in circular Bil (30) BPFK/PPP/01/03, 13 th May 2009, punitive action shall be takenagainst companies who are involved in adulteration.Any registered products found to have been adulterated, the following action shall be takenby the Director of Pharmaceutical Services:a) The registration of the related product shall be cancelled and recall of all batches ofthe product shall be done immediately;b) The manufacturer‟s license of the related manufacturer shall be revoked for six (6)months for the first offence and one (1) year for the subsequent offence, from the dateof revocation letter;c) All transactions (including application for product registration, application for change ofproduct registration holder, application for change of manufacturing site) for theadulterated product registration holder shall be frozen for six (6) months for the firstoffence and one (1) year for the subsequent offence, from the date of cancellationletter from the Authority.National Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 119
Page 2 and 3:
Drug Registration Guidance Document
Page 5 and 6:
Page 7 and 8:
Page 9 and 10:
Page 11 and 12:
Page 13 and 14:
Page 15 and 16:
Page 17 and 18:
Page 19 and 20:
Page 21 and 22:
Page 23 and 24:
Page 25 and 26:
Page 27 and 28:
Page 29 and 30:
Page 31:
Page 34 and 35:
Page 36 and 37:
Page 38 and 39:
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: Drug Registration Guidance Document
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?