1. SEARCHING OF FILES FOR NEW PRODUCT DEVELOPMENT IN REFERENCE GOOGLE AND OTHER WEBSITES
2.NEW FILE MUST BE PREPARED IN ACCORDANCE WITH THE RELEVANT SAMPLE FILES
3.MAILING TO FDA REGARDING PERMISSION COPY
4. PREPARATION OF WORD FILES IN ACCORDANCE OF THE ART WORK PREPARATION OF BOX LABEL,STRIP,INSERT,LITERATURE,ETC.AND FORWARD IT TO DTP DEPARTMENT FOR DESIGNING
5. ON RECEIPT OF ART WORK FROM DESIGNER WE DO PRIMARY CORRECTION OF ART WORK
6.AFTER PRIMARY CORRECTION FILE IS FORWARDED TO FDA, Q.C. & Q.A FOR THEIR VERIFICATION & SIGNATURE
7. ON RECEIPT OF CORRECTED FILE NECESSARY CHANGES IS TO BE MADE BY DTP PERSON 8 FINAL COPY SHOULD BE SEND AGAIN FOR FINAL VERIFICATION BY ALL DEPARTMENTS HEAD
9 TAKE OUT P.O. FROM DTP DEPARTMENT & SEND THE FILE TO PACKING IN CHARGE FOR PRINTING PROCESS
10. FINALLY SEND THE FILES FOR ENTERING THE MASTERS FOR RESPECTIVE PRODUCTS TO THEIR CONCERNED DEPARTMENT.