Why do you need us?

3he pharmaceutical and 4iotech industries are gro)ing at an e5tremely high rate, and )ith e#eryone trying to catch the ne5t )a#e to 4e the leader in the industry, it6s no surprise that the need for Validation has increased$ So, )hy do you need us7 Azzur is proficient at la4oratory and manufacturing e8uipment #alidation, cali4ration, analytical e8uipment #alidation, process #alidation, computer system #alidation, cleaning #alidation, and other supporting re8uirements for facilities and la4oratories that maintain a 8uality management system and adhere to (ederal *egulations$ +hether you are *&9 or Manufacturing you ha#e to comply )ith regulations ensuring the safety and efficacy of your product$ :ere are ;ust a fe) )ays )e at Azzur, can help you$ G9!, or Good 9ocumentation !ractices are procedures that are created and maintained 4y your site$ Azzur pro#ides the most current training to all of its employees to ma<e sure that, prior to your arri#ing on your site= they are prepared to create documents, perform testing, and document the results to meet cGM! and G9! standards$ Commissioning and *is< Assessments are 4asic standards that e#ery site needs$ y pro#iding commissioning efforts and ris< assessments, )e help to ensure that all systems and components of a site or plant are put together accurately )ith minimal ris< in#ol#ed so that )e meet all the essential needs to ha#e a pro;ect run smoothly, 4oth on time and 4udget$ Cham4er Validation and Analytical >8uipment Validation has 4ecome an increasing demand due to more research 4eing performed and products 4eing created in the pharmaceutical industry$ :ousing products at certain temperatures and maintaining consistent sta4ility at those temperatures, along )ith ha#ing the proper functional e8uipment to test these products, is a M?S3 if you are going to ha#e your product reach human use$ :a#ing your e8uipment #alidated )ill pro#e to the (9A that you are the right trac< to ma<ing sure your product is safe and ready to sa#e li#es$ Cleaning #alidation procedures ensures that your e8uipment, tan<s, and lines are clean and safe during your manufacturing processes$ !rocess Validation ensures that your manufacturing processes, from the design stage all the )ay throughout production, are capa4le of consistently deli#ering 8uality products$ 9uring manufacturing of products you al)ays )ant to 4e sure that your #essels, pipes, filters, and other process e8uipment are clean$ C"! @Clean "n !laceA is a method of cleaning that allo)s you to clean your closed systems at the end of production 4efore you start up another 4atch, or do another transfer )ithout disassem4ling and manually cleaning the parts of the soilant$ 3an< S"! @Steam "n !laceA is important 4ecause you are sho)ing that you ha#e a method of sterilizing your e8uipment to ensure that )hen you put ne) product through it, it )onBt 4ecome contaminated$ Azzur Group, LLC is a lifesciences consulting firm specializing in Mechanical C&Q, Computer System Validation, Audit and Compliance, and usiness !rocess "mpro#ement$ Azzur Group LLC is confident that )ith the right employee@sA and the right commissioning plan, )e can help your company gro) to 4ecome a true competitor in the 4iotechnology and pharmaceutical industry$ +ith successful pro;ects in Maryland, !ennsyl#ania, Massachusetts, 3e5as, California, "reland, >ngland, and many more, )e feel )e can pro#ide you )ith the <no)ledge, respect, and integrity to get your pro;ect completed to your company standard$

Azzur Group, LLC %&' (itz)aterto)n, *d$ +illo) Gro#e, !A ,-.-. ,-&,/-0&&-10&& info2azzurgroup$com )))$azzurgroup$com