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ABOUT US

Mediflow Pharmaceutical (Pvt) Limited

Mediflow Pharmaceutical (Pvt) Limited was established in 2014 and is a subsidiary of Ahbab Associates. Our founder company has been in the business of engineering, logistics and construction project management for the last 5 decades. Since its inception Mediflow Pharmaceutical has expanded its manufacturing facility, shared its expertise and knowledge of experience in health care delivery sector such as hospitals and healthcare education.

ABOUT US

Mediflow Pharmaceutical (Pvt) Limited

Mediflow Pharmaceutical (Pvt) Limited was established in 2014 and is a subsidiary of Ahbab Associates. Our founder company has been in the business of engineering, logistics and construction project management for the last 5 decades. Since its inception Mediflow Pharmaceutical has expanded its manufacturing facility, shared its expertise and knowledge of experience in health care delivery sector such as hospitals and healthcare education.

25

Years Of Experience

638

Successful Projects

125

Team Members

500

Happy Clients

Major Hazards of
Conventional I.V Bottles

Sterility

(Sterilized at 106 C only due to LDP material)

Permeable Shape & Opacity

(Unclear Bottles, Unsmooth Surface, Leachable)

Neck Leakage

(Nipple Top Single Insertion Point Bottles)

Need Pricking for Air Venting

(Non Collapsible Bottles)

Need Pricking for Admixing

(No Insertion Point for Admixing)

Logo Blue Tagline

Proudly Introducing
Flow-MTZ 100 ml

Mediflow is the first and only European Poly propylene L.V.P

unit in Pakistan with all range euro cap & 100% Auto Particle

inspection.

MEDIFLOW'S IV
Infusions in PP Bottles

Mediflow’s I.V bottles are manufactured using Polypropylene (PP) 1. An FDA-approved medical grade and meets…

CONVENTIONAL I.V
Infusion LDPE Bottles

Conventional I.V bottles are manufactured using Low-density poly-ethylene (LDPE). Which is the world being over widely replaced by…

BIBLIOGRAPHY
  1. SCG. SCG Chemicals. [Online] SCG. [Cited: march 5, 2014.] meets all the requirements of international safety standard for medical devices including US Class VI, EP method and U.S. FDA 21 CFR 177.1520 for I.R. and I.V. solution bottle with Autoclave sterilization.
  2. Pharmaceautical Packaging: Current Trend and Future. Khunteta, Vikas Pareek and Dr Alok. 2014, International Journal of Pharmacy and Pharmaceautical Sciences (vol 6), Vol. 6, p. 1.
  3. WHO. WHO guidlines. GENEVA : World Health Organisation, 2002.
  4. AIR MIXING with IV fluids and Injections. LODHA, RAKESH. New delhi : Indian Pediatrics, 2010, Vol. 47.
  5. Integrated Medical Industries (IMI). IMI. [Online] IMI, 2010. http://www.imi.com.ng/assets/downloads/productdetails.pdf.
  6. convention, UNITED states Pharmacopeial. The united states pharmacopeia. s.l. : The united states pharmacopeia, 2014.
  7. Health, Great Britian Department of. Methods of Sterilisation. BRITISH PHARMACOPEIA. london : Great Britian Department of Health, 2015, Vol. 5.
  8. Vibhakar Shah, Ph.D. Inhalation Drug Products in LDPE Containers: A quality (CMC) Perspective. FDA. [Online] may 05, 2004. [Cited: may 10, 2010.] www.fda.gov/ohrms/dockets/ac/04/…/2004-4040S1_02_FDA-Shah.pp.