Unicare is dedicated to partnership and team work, a company that pairs the best of experience to the needs of Cosmetics & Health care products. the.

Slides:



Advertisements
Similar presentations
Software Quality Assurance Plan
Advertisements

Radiopharmaceutical Production
Update on Penn Pharma John Roberts, Commercial Director December 2012.
Gaining a Competitive Advantage
DPS 304 : Purchasing /Procurement Activities
Industry's Role in Promoting Best Practices A Collaborative Approach to Food Safety Global Food Safety Policy Forum Washington DC September 16, 2011.
More CMM Part Two : Details.
ORGANIZATION. 2 Problem scenario  Develop an organizational chart for your laboratory showing lines of authority from the head of the organization to.
How to Document A Business Management System
Public and Private Interests in Animal Research LAT Chapter 1.
INDUSTRIAL & SYSTEMS ENGINEERING
Operations and Service Management Chapter 21. Copyright © 2005 by South-Western, a division of Thomson Learning. All rights reserved. 2 Operations and.
College Strategic Plan by Strategic Planning and Quality Assurance Committee.
Dar Al Dawa Veterinary & Agricultural Industrial Co.
Center for Health Care Quality Licensing & Certification Program Evaluation 1 August 2014 rev.
DRIVING INNOVATION AND ABILITY TO COMPETE THROUGH OUTSOURCING Anthony (Tony) C. Bernardo, Alloy Polymers Inc. NPE 2003 bernardo:
ISO 9000 Certification ISO 9001 and ISO
Laboratory Information Management Systems (LIMS) Lindy A. Brigham Div of Plant Pathology and Microbiology Department of Plant Sciences PLS 595D Regulatory.
The “ Operon Strategist” is working towards the catalyzing and ensuring the strategic development of the clients in the areas of Regulatory approvals,
LIFE SCIENCES Pharmaceutical Manufacturing Chemical & Biosciences Technology QA/QC in Pharmaceutical Industry Applied Biology & Chemistry.
Devahuthi Software Solutions Pvt Ltd. About Us Devahuthi Software Solutions is a global PLM Consulting, Technology services provider and Outsourcing company.
UNIT 3.04 Career Opportunities By PresenterMedia.comPresenterMedia.com.
Personnel Basic Principles of GMP Workshop on
ISO 9000 Implementation Imran Hussain.
ISO 9000 Introduction Imran Hussain.
Director's Message Suri Auto Pvt Ltd is the name made to be the best, by hard work, dedication and team spirit; the highlights that enhance our ongoing.
Visit us at E mail: Tele:
Documentation –Part 2 Basic Principles of GMP Pharmaceutical Quality,
Creating Lasting Change for Your Business ISO 9001:2000 Management System Overview.
Regulatory Overview.
ASEAN GMP TRAINING MODULE PERSONNEL
Introduce on Imported Foods System in Korea - Under The Food Sanitation Act - Korea Food and Drug Administration.
Target Institute of Medical Education & Research (TIMER) Provides Clinical Research services to Pharmaceutical, Biotechnology product companies right.
Presentation of HanKing
Industrial Engineering Roles In Industry
Advice for Internal Compliance Programmes Billy Au Principal Trade Officer Head of Strategic Trade Controls Branch Trade and Industry Department The Government.
Inspection of Blood Establishments. GROUP 1 First, we would like express our sincere thanks and appreciation to our friends and colleagues from IBTO for.
Prepared by the (Institute of Industrial Engineers – Industry Advisory Board)
COMPANY PROFILE.
Important informations
MEDICAL experts INDUSTRY Some of our clients. Pharmaceutical companies, manufacturers of medical and surgical devices, clinical research organizations,
This class cannot be shared or copied without the written permission of PracticeWorks Systems, LLC.
Basic Principles of GMP
Unicare is dedicated to partnership and team work, a company that pairs the best of experience to the needs of Cosmetics & Health care products. the.
Pharmaceutical Quality Control & current Good Manufacturing Practice
SEN 460 Software Quality Assurance. Bahria University Karachi Campus Waseem Akhtar Mufti B.E(C.S.E) UIT, M.S(S.E) AAU Denmark Assistant Professor Department.
Producing a Pharmaceutical or Biopharmaceutical The Manufacturing Process.
1 QUALITY MANAGEMENT SYSTEM PRESENTATION TO BOTSWANA DRUG ADVISORY BOARD MEMBERS 13 th – 17 th AUGUST 2007.
CM&C Inspections The Pre-Approval Inspection (PAI) in the US 27 May 2010.
Al Noor Drug Store Amman- Jordan Established in 2001.
ITRI Industrial Technology Research Institute The Audit Process of Medical Device GMP for Domestic Manufacturers DOH Designated Auditing Organizations.
Department Of Pharmaceutics. PRODUCTION It is a process or procedure of converting a set of inputs, namely men, capital, information & energy into finished.
ISO Certification For Laboratory Accreditation ISO Certification For Laboratory Accreditation.
GOOD MANUFACTURING PRACTICE FOR BIOPROCESS ENGINEERING (ERT 425)
An Introduction to Advik Laboratories Ltd
ISO/IEC
Quality Assurance and Quality Control in Generics
Industrial Pharmacy.
Good Clinical Practice
Lesson 5: BRITE Seminar: GMP II
GFSI Certification What Top Management Needs to Know
Bio-Facility Qualification, Start-Up & Licensure
Producing a Pharmaceutical or Biopharmaceutical
JYOTI CAPSULATIONS PVT. LTD.
INTRODUCTION HISTAR INTERNATIONAL LIMITED Tel.: Fax: Nov 28, 2016.
UNDERSTANDING FOR STANDARD
UNIT 1 B ROLE OF ENTREPRENEUR.
Preparation for Third Party Audit
ISO 9001:2000 Management System Overview
Radiopharmaceutical Production
Presentation transcript:

Unicare is dedicated to partnership and team work, a company that pairs the best of experience to the needs of Cosmetics & Health care products. the customers we serve today and will serve tomorrow.

Creating value for our customers by providing worldwide professional Cosme ceutical preparations & services that translate leading edge of technological and scientific advances into practice.

We pride ourselves in having a Scientifically focused staff that will dedicate itself to understanding the scientific, medical and practical concerns about our products

Philadelphia Pharmaceuticals: 1.. Initially working as quality control analyst in the instrumental laboratory HPLC Lab 2. Taking major part in raw materials, packing materials & finished products analysis 3. Establishing the Microbiology Lab & establishing SOPs for all related tests ( MLT, STERILITY. LAL, CHALLENGE TEST, MIC MBC …..etc) 4. Playing major role in formulation Departments / suspensions, semisolids & liquids 5. Playing major role in methodology department & carry out all method validation 6. Playing major part in stability division & maintaining all stability records 7. Taking part in validations team & establishing the SMPs for new products 8. Establishing software based on Visual Fox Pro Version 5.0 to conducts & maintain all technical responsibilities ( building the flow charts & the ERD) 7. Preparatory of all registration files inside & outside the kingdom & following up all these file requirements in the central lab of medicine analysis 8. Membership in steering committee meeting for the R& D Department 9. Playing main role in ISO 9002 certificate acquirement & preparatory of Manual. Policy, QPs, SOPs & WIs

Avalon Pharmaceuticals Establishing the factory & building the layouts, materials & personnel flow diagrams & following up all related construction works & leading the responsible team against the MOH inspection visits & supervision until GMP certificate has been got. Production Manager ( getting all production machines & assembling & installation of those machines & lead to productive stage Purchasing all required raw materials & packing material from Overseas & following up all pricing, shipment & clearance details Building the Quality & Development Laboratory & getting all the required instruments (HPLC, Spectrophotometer, Titrators …..etc) Building all required SOPs for Quality control Department Head of Product Development Department & formulating more than 20 products ( mouthwash, antiseptics, creams, ointments, gels & lotions Registration of products in MOH & follow up all registration details Having major part in steering committee meeting Building the Quality assurance Department & establishing all required procedures( Document Control. Internal Auditing, Management Review system.Problem Reporting…..etc)

Saudi Pharmaceutical Industries Supervision & leading the company to register two new production lines ( Injections & Semisolids) Building all the required system & procedures for all the departments ( Quality Assurance, Quality Control, Production, stores & Purchasing etc ) Developing new software for the company which controls the mission of the technical department through ORACLE BASED SYSTEM ( Working for around 1.5Year ) We are now preparing to register new line for human products Taking the complete care of planning Department & building all the production planes ( monthly planes as per Sales Department Feedback ) Follow up the (Production. Quality Control, Quality Assurance, stores & PD ) Registration of the company products for both veterinary & Human Products )

Unicare cosmetics was established in The company was established to capitalize on the surplus demand for contract manufacturer in the cosmetics industry in Kingdom Of Saudi Arabia. Unicare cosmetics started out as small scale cosmetics contract manufacturer for various brands in the local market with a number of employees of less than 5. After one year, Unicare cosmetics had grown rapidly and now Unicare cosmetics has good experience in OEM of cosmetics. To be the leading contract manufacturer in K.S.A Unicare had materialized it by upgrading its factory to GMP (Good Manufacturing Practice) status by the construction of a modern factory to meet with to Rules and Regulations of SFDA in Saudi Arabia for cosmetics manufacturers. All products produced by our factory can be exported to all the surrounding countries freely. As part its business expansion plan,

Unicare cosmetics also invests in the expansion of production capacity, modernization and upgrading of production facilities, and implementation of automation production. The total turnover of Unicare Cosmetics for year 2009 is 5 million Saudi riyals. Unicare foresee its turnover to increase further with the expansion of its market share UNICARE has a longstanding commitment to high quality. There is ongoing investment of training of personnel and the dynamic improvement of services. UNICARE assures : - Fast recruitment of qualified volunteers - Quality in every aspect of work - A team of experts with high degree of experience & ethics - Delivering on commitment

Due to the rapid increase of our business volume & after having a lot of inquires which cannot be executed in the exsisting facility we decided to start our new facility in the second industrial area in Riyadh. the new plant will be composed of three level 1000 squared meter building in 2000 squared meter land. & the execution of this project is divided into Two stages as follows :