Multilocational details

Name & Address
Telephone No.
Fax No.
Contact Person
Email ID
Head Office
ACG Associated Capsules Pvt.Ltd.
Plot No. 131, Kandivali Industrial Estate, Kandivali (West), Mumbai-400067, India.
+91 22 71948400
Patricia Shetty
Vice President-Global Quality and Regulatory Affairs
ACG Associated Capsules Pvt.Ltd.
131, Kandivali Industrial Estate, Kandivali-West, Mumbai-400067, Taluka: Kandivali West, District: Mumbai-Zone 7, Maharashtra, India.
+91 022 71948600
Sunil Sadekar
Quality Head
ACG Associated Capsules Pvt. Ltd.
Ashagadh, Dahanu Road, Dahanu -401602, Taluka: Dahanu, District: Thane-Zone 4, Maharashtra, India.
+91 2528 260131/ 32/ +91 75070 44561/ 62
+91 2528 260173
Paschal Vaz
Quality Head
ACG Associated Capsules Pvt. Ltd.
GAT NO. 322, 323 AT.-Shindewadi, Post-Shirwal, Taluka-Khandala, Dist.-Satara.,Pin Code – 412801, Maharashtra, India.
+91 7720089461/462/463
Khailan Shaikh
Quality Head
ACG Europe d.o.o
ACG Europe d.o.o. Frankopanska 79, 42230 Ludbreg, Croatia
+385(42)660118 /+385(98)435127
+385 (42) 660 130
Andreja Makar
Quality Manager
ACG Associated Capsules Pvt.Ltd.
Plot No.M-29-M-44, Phase II, Pharma Zone, SEZ, Pithampur, Dhar (MP)- 454775, India.
+91 8818883901/3902/7740/7741/7742/7743
Yogesh Mahanubhav
Quality Head




The site is located in a pollution free environment away from potential sources of dust; smoke foul odours and other types of contamination. The manufacturing facility is designed, constructed and maintained to facilitate the manufacturing of hard capsule shells under hygienic conditions. It conforms to the conditions laid down in the Factories Act 1948.

Define batch?

A specific quantity of material produced in a series of processes and expected to be homogeneous within specified limits.

What is batch size?

Minimum: 1 million capsules Maximum: 10 million capsules

Define batch numbering system?

A typical batch number consists of system generated (SAP) 10 digits, where first 4 digits indicate the manufacturing location while the remaining 6 digits are serial numbers.

Ex. 1100000278

1100  -   Dahanu location

1110  -   Kandivali location

1120  -   Shirwal location

1150  -   Pithampur location

4100  -   ACG Lukaps location

4720  -   ACG do Brasil S/A


Training Program

Personnel suitably qualified through education, experience and training are engaged in the manufacturing, processing, packaging, distribution and quality assessment of empty capsules.


All new employees are put through an induction program of appropriate duration depending upon their grade, position and nature of work. Departmental orientation is provided by the HOD and section in charge.


Training on GMP, hygiene, sanitation and SOPs is conducted for all employees whose work impacts quality of the product. In addition personnel are counselled and trained on safety practices, fire fighting and first aid.


Training needs of management and supervisory personnel are identified by the HODs based on qualifications, experience and nature of responsibilities. Management personnel are also evaluated annually for performance and any evident training needs are identified. Training needs for each category of workmen and staff are identified by HODs as per the nature of work carried out. These are recorded in the training need identification form.


A training calendar for internal and external training is drawn to incorporate training for all identified needs and training is provided. Hands on experience is given where necessary. Evaluation is done through objective test or on the job observation and this forms the basis for identification of retraining needs. Training details are recorded in the individuals training card which is maintained by HR department in the employees personal file.

Cleaning & Sanitation

A written housekeeping program is set up, assigning responsibility for sanitation. It outlines the cleaning schedules, methods, equipment and materials to be used in cleaning. Only approved cleaning and sanitizing agents are used.


The entire factory has been grouped into following categories:


  • Critical areas: Mucilage preparation, Hard Capsule Machines & Printing

  • Important areas: General stores, Final Quality Control Dept., Finished goods store, Work In Progress site, Production corridors and immediate surrounding areas, staircases, laboratory etc.

  • Service Areas: Non - production corridors, offices, canteens etc.

  • Surrounding: Compounds, Utilities etc.

  • Toilets


Cleaning involves a general cleaning for all non-critical areas & specialized cleaning for critical areas.


General cleaning for non-critical areas are done by using wet mopping with disinfectant solution such as solution Phenyl for general cleaning & Sodium Hypochlorite (2%) in change room.


Specialized cleaning for critical areas are done by using mopping with disinfectant solution such as Virosil, Polysan, Protasan, Sumabac, Sodium Hypochlorite.


Compositions are provided below:


  • Virosil - Hydrogen Peroxide stabilized with Silver ions.

  • Polysan - Iodophor containing tamed Iodine.

  • Protasan - Fatty alcoholethoxylate, Quaternary Ammonium compounds, Benzyl - C12 - 16 - Alkyldimethyl Chlorides, Editic acid, Betain.

  • Sumabac - Alkyldimethylbenzyl ammonium chloride, Alkylalcohol Ethoxylate, Sodium carbonate.

Pest control program

A Pest Control Program encompasses the entire facility and premises on a regular basis to prevent any insect or rodent infestation.


Pest control is done to keep the factory free from pests, rodents and insects. Quotations are invited from various pest control agencies and they are short listed on the basis of their performance and experience. A contract is signed with the agency to undertake pest control as per technical agreement.


The effectiveness of pest control is monitored fortnightly. In case of ineffectiveness, the agency is called for investigation of cause and corrective action / measures are implemented.


Flycatchers are installed in all critical areas. Cleaning of insectocutors is done once 15 days.

Preventive maintenance program

The maintenance department in conjunction with the user departments is responsible for maintenance of production and testing equipment. Preventive maintenance  schedules are drawn for hard capsule manufacturing machine and accessories, gelatin room equipment and capsule printing machines based on their impact on equipment continuity and product quality. These are implemented and monitored.

Validation policy

Process Validation is defined as the process of establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality attributes.

Before process validation can begin, the facilities, equipment, and utilities that will be employed for the process validation activities must themselves be qualified.

Analytical testing methods are validated. Staff taking part in the validation work are appropriately trained.

Stability program

We perform stability study at following condition as per ICH guidelines and conducted on 3 batches per year.

  • Long term stability study: Recommended storage condition of Hard Capsules Shells, Room temperature between 15°C to 30°C and 40% to 65% RH.
  • Short term stability study: 30°C ± 2°C and 65% RH ± 5 %.

Who has responsibility for releasing raw materials, packaging materials, intermediates, finished goods and what is the routine procedure for these activities(e.g.ID test etc.)?

Raw materials, packaging materials, intermediates & finished goods are tested by QC chemist & approved by Head QA in SAP. Test data is entered into SAP. QA responsible person reviews the data & BMR & releases the materials by giving usage decision in SAP.

Is release process via a validated computer system?

Yes validation report no VR/PQ/SAP/01/01 dated 28/1/12.

Describe customer complaint handling?

Customer complaints are received by sales team and recorded in the SAP system from where they are forwarded to QA. Complaint is investigated, evaluated and a corrective action is identified. Customer is informed regarding the outcome and corrective action initiated to prevent reoccurrence.

Change control program

Identify area of Improvement (Seek Approval)

Authorize Trials (Release trial approval )

Conduct Trials as applicable and Validate

Inform customer through formal change control for significant changes which may affect product quality

Implement Change

Monitor & Review changes implemented

Handling of nonconforming products

Nonconforming raw material, packaging material, in process material and finished product are identified, documented and segregated to prevent their inadvertent use.

Nonconforming material is disposed off by one of the following ways as appropriate and concern functions are notified

a) Rework to meet the specified requirements

b) Accept with or without rework by concession

c) Re-grade

d) Scrap or reject

Non conforming products are isolated physically as well as by computers

Handling of out of specification

In the event that a result of a test does not conform to specifications, when performed for the first time, describe what action is taken.

1) Immediate supervisor is informed.

2) OOS investigation starts as per OOS SOP and protocol.

3) Retests are performed if OOS result is invalidated by evidence. Retest is performed on the same sample.

4) Production review done if no assignative cause is found.

5) Verdict.

Handling of deviation

1) Planned deviations involving change in process or systems are handled through Change Control and monitored.

2) In case of unplanned deviation (e.g. Power fluctuations in Mfg. Area) the person who observes the deviation informs the observation immediately to his Supervisor. Supervisor inform HOD-QA and raise the deviation form. HOD- QA or his representative visits the site of deviation and record their observations. Cause of deviation is investigated and actions are planned for correction of the same. Completions of correction activities are monitored.

What percentage of your business is for the pharmaceutical & nutraceuticals?

80% for pharmaceutical and 20% for nutraceuticals.

Retention period for preserved samples & batch records?

6 years (5 Years expiry +1 Year in archive area).

Are you division or subsidiary of another company?

Yes, we are division of ACG Worldwide.

Production capacity utilization


Date of Establishment

Kandivli - 12 July 1961 
Dahanu - 2 May 1983  
Shirwal - 20 September 1994
Pithampur - 7 August 2013 
ACG Europe d.o.o. - 1 June 1981
ACG do Brasil S/A - 24 December 2018



Installed capacity as on March 2022

Hard Gelatin Capsule Shells

Dahanu - 33.79 billion per annum

Kandivli - 16.76 billion per annum

Shirwal - 22.46 billion per annum

Pithampur -  19.83 billion per annum

ACG Europe d.o.o - 17.42 billion per annum

ACG do Brasil S/A - 12.65 billlion per annum

Total - 122.91 billion per annum


Cellulose Capsule Shells

Dahanu - 5.55 billion per annum

Pithampur - 10.25 billion per annum

Total - 15.80 billion per annum

Last date of FDA inspection by local authority

Dahanu –  24 August 2020

Shirwal – 12 March 2021

Kandivali – 25 March 2021

ACG Europe d.o.o – 23 to 25 August 2021

Pithampur - 23 & 24 September 2019

ACG do Brasil S/A- 28 June to 02 July 2021

Commercial Details

Excise Duty ECC No.
Chapter I.D number for EHGC/HPMC
Factory Registration No.
Import Export Code Number
Excise Tariff No. 2
Excise Tariff No. 1
Excise Collectorate
Excise Division
Excise Range
Chapter I.D Subheading
AAA CA 4769KXM001
Cellulose Capsules 96 02 00 90
Gelatin Capsules 96 02 00 30
AAA CA 4769 K, ACG Lukaps - 95072828169
27710000091C Dated: 01/04/06
Mumbai - V
Gelatin: 96020030, Cellulose: 96020090
AAA CA 4769KXM003
Thane - II
Boisar II
Gelatin: 96020030, Cellulose: 96020090
AAA CA 4769KXM002
Gelatin: 96020030, Cellulose: 96020090
Not applicable being special economic zone
Pithampur : 39/D-149/ISEZ/2013
Cellulose Capsules 96 02 00 90
Gelatin Capsules 96 02 00 30
AAA CA 4769 K
23519039762 Dated 09/02/2012
Not applicable being special economic zone
Not applicable being special economic zone
Not applicable being special economic zone
Gelatin: 96020030 Cellulose : 96020090

Number of Employee in manufacturing facility

Sr. No. Department Kandivali Dahanu Shirwal ACG Europe d.o.o Pithampur
1 Gelatin Room 28 55 35 41 23
2 Production 46 76 48 37 73
3 Utility 21 35 40 19 26
4 Purchase 1 1 1 6 2
5 Stores 4 5 7 9 6
6 PFD 42 170 88 55 112
7 QA / QC 47 80 50 43 72
8 HR & Admin 5 7 5 3 5
9 Projects 1 0 0 2 1
10 Accounts & Excise 1 0 1 5 3
11 Maintenance 17 36 0 20 28
12 HOC 3 4 4 0 4
13 IT - 1 1 2 1
14 HPMC - 34 CIC 4 0 23
15 Sales & Marketing - - - 9 -
Total 216 504 280 251 379

Complete facility area in square meter

Total Area of Plot
Total Built Up
Factory (131) Stores & IT (145) Commercial (130)
4933 1440 895
6071 1114 826
0 326 69
ACG Europe d.o.o

Department area of manufacturing facility in square meter

Sr. No. Department Kandivali Dahanu Shirwal ACG Europe d.o.o Pithampur
1 Gelatin Room 259 1350.52 3320.33 883,44 548.33
2 Production 1638 3593.92 6340.44 1672 701.50
3 Utility & Maintainance 2210 1891.53 7817.12 4497 1046.4
4 Stores 1114 904.64 632.75 1554 298.6
5 PFD 1592 3281.21 1571.20 1203 1811.97
6 QA / QC 230 377.50 472 828 431.22
7 HR & Admin 86 681.66 1175 47,61 130.69
8 Sales & Marketing 424 - - 66,74 -