Chemical Pharmaceutical Research Institute, nihfi, Bulgaria, Process Development, Scale-up Analytical,  Methods Development, Validation Stability Studies, Organic Synthesis, Drug Master Files, Pharmaceutical Intermediates, Bulk Pharmaceutical, Chemicals, Toll Synthesis, Fermentation, Downstream Isolation, Microbial Products, GMP, Dosage Forms Facilities, Scientific, Technical, Economical, Patent, Synthesis, Galenica, Oral Cavity, Natural Products , Microbiological, Biosynthesis, Environmental Care,  Analgetics, non-narcotic, tempalgin, ulcer, Ranitidin, Roxatidin, narcotic, stobium, anxiolitic, alprazolam, Rudepam, antihistamatic, allergic, astmasol, bicromat, clemastin, clenbuterol, Idumed, ketotifen, cardiotonic, digoxin, dobuxan, antiarrithmic, propranolol,  verapamil, chemotherapeutic, sulfaprim, antibiotic, amikacin, bactroban, choleretic, hymecromon, diabetic, glibenclamid, mucarthrin, levamisol, acnederm, fenofibrat, diuretic, fupiram, hypertensive, captopril, clonidon, Nifedipin, prazosin, propranolol, verapamil, carsil, migraine, cinergin, dihydroergotamin, ergotamine, levamisol, antimycotic, nizoral, motilium, tamoxifen, neopredin, ginvasin, antiherpin, Bebogel, Parkinson, prolactin, bromocriptin, neuroleptic, haloperidol, rheumatic, piroxicam, methylergometrin, ergotamine, monisid, nifedipin, propranolol, sydnopharm, cinnarizin, broncholytin, troxevasin, Azatadine, Bismuth Subcitrate, Colloidal, Cetirizine, Dobutamine, Fentanyl, Flunarizine, Ketotifen, Lobenzarit, Methotrexate, Moclobemide, Nicorandil, Pefloxacin, Prazosin, roxatidine
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Complete research and technological cycle:
  • Scientific, patent and trade information concerning world-wide leading research projects and achievements in the pharmaceutical, biotechnological and chemical industries;
  • R & D projects in the field of organic synthesis, biosynthesis, isolation and purification of bioactive substances; oral hygiene and stomatological therapeutical products ; pharmaceutical analysis
  • Optimization of technologies in the chemical-pharmaceutical and microbiological industries;
  • Development of technologies for production of dosage forms for human and veterinary practice;
  • Transfer of technologies and delivery of licences;
  • Search and study of new indications for already approved and approbated substances and dosage forms;
  • Design, synthesis and screening of bioactive substances;
  • Full preclinical, medical biological characterization of drugs and preparation of Drug Master Files for registration in the country and abroad;
  • Production of small batches of drugs based on our own or licence technologies by using modern technical equipment under the GMP conditions.

05/11/2004

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